High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results
© Siggberg et al.; licensee BioMed Central Ltd. 2012
Received: 30 May 2011
Accepted: 5 September 2012
Published: 17 September 2012
Diagnostic analysis of patients with developmental disorders has improved over recent years largely due to the use of microarray technology. Array methods that facilitate copy number analysis have enabled the diagnosis of up to 20% more patients with previously normal karyotyping results. A substantial number of patients remain undiagnosed, however.
Methods and Results
Using the Genome-Wide Human SNP array 6.0, we analyzed 35 patients with a developmental disorder of unknown cause and normal array comparative genomic hybridization (array CGH) results, in order to characterize previously undefined genomic aberrations. We detected no seemingly pathogenic copy number aberrations. Most of the vast amount of data produced by the array was polymorphic and non-informative. Filtering of this data, based on copy number variant (CNV) population frequencies as well as phenotypically relevant genes, enabled pinpointing regions of allelic homozygosity that included candidate genes correlating to the phenotypic features in four patients, but results could not be confirmed.
In this study, the use of an ultra high-resolution SNP array did not contribute to further diagnose patients with developmental disorders of unknown cause. The statistical power of these results is limited by the small size of the patient cohort, and interpretation of these negative results can only be applied to the patients studied here. We present the results of our study and the recurrence of clustered allelic homozygosity present in this material, as detected by the SNP 6.0 array.
KeywordsDevelopmental disorder SNP array Diagnostic yield
The diagnostic yield of microarray comparative genomic hybridizations (array CGH) has already proven to exceed that of cytogenetic methods, except when it comes to balanced rearrangements. A consensus statement suggests that microarrays should be used as the first line of testing for developmental disorders of unknown cause . However, as our previous study shows, approximately 80 % of patients with a developmental disorder of unknown cause (mental retardation and/or malformations and/or neurological disorders) remain undiagnosed even by array CGH analysis (44 K, 180 K, or 244 K) . Thus, other methods are clearly needed to define the pathogenic mechanisms. It is plausible that small copy number variants (CNVs) may go undetected if the probe coverage is limited, as it may be in low-resolution arrays. By increasing the resolution, one would thus expect to detect increasingly smaller pathogenic CNVs.
The frequency of uniparental disomy (UPD) in newborns is reportedly ~0.029% . Around 1,100 cases of whole chromosome UPD and some 120 reports on segmental UPD are described in the literature . Some recessive diseases are expressed in children who have inherited the mutation form a single carrier parent . The explanation for this is a meiotic or very early mitotic recombination event between parental homologous chromosomes causing segmental UPD of the genomic segment containing the mutation, and thereby causing a reduction to homozygosity.
As the market is flooded with new arrays, most having an increased resolution and a promise of ever higher detection rates, the question remains what the added value is of these ultra-high resolution arrays. To test this, we used an array with 1.8 million probes and an average resolution of 0.7Kb to analyze samples of 35 patients with developmental disorder of unknown cause, normal karyotype, and normal array CGH results by use of Agilent 44 K, 180 K, or 244 K platforms (Agilent Technologies, Santa Clara, CA, USA).
Clinical characteristics of patients studied
Head and neck
Eyes and vision
Ears and hearing
Skeletal and limb defects
Postaxial polydactyly (one foot) Short meta-carpals V finger clino-dactyly
Severe DD No walk/crawl No speech Epilepsy Drooling
Dolicocephaly Narrow, prominent forehead Low, uneven hairline
DD Abnormal pons
Low nasal bridge
Horseshoe kidney Anal atresia
Small hands and feet
Thick and straight eyebrows Broad nasal bridge Long philtrum Retrognathia
Autism ID Epilepsy
Blindness Optic nerve hypoplasia
ID Epilepsy Severe hypotonia
Brain malformation Severe DD
Small nose Low nasal bridge Tented upper lip
Severe DD Severe epilepsy
Severe optic atrophy Impaired vision
ID Epilepsy Cortical atrophy
Triangular face Small jaw High palate Thin upper lip
ID Autistic features Intractable epilepsy
Frax-dna, SCN1A, CLN8 4p-FISH normal
Upslanting palpebal fissures
ID Autistic features Intractable epilepsy
ID Autistic features ADHD
Balanced t(2;9)(q13q22.3) de novo
Severe ID Hypotonia Autism Epilepsy
Inv 2(p13p25) mat., DMPK mutation negative
Severe myopia Cataracta
Synophrys Curved eyebrows Upturned pinched nose Big mouth Full lips
Atrial septum defect
Severe DD Epilepsy
Ventricular septum defect
ID Beahvioural disturbances Autism
No malformation or dysmorphism
Mild ventricular septum defect
19. & 20.
No structural defects
Small nose Low nasal bridge Smooth philtrum Thin lips
Proximal thumbs Pes planus
ID Intractable epilepsy Ataxia
Pre- and postnatal growth retardation
Broad nasal root Short nose Bifid nasal tip
Cryptorchidism Hypoplastic scrotum
Slow motor development Hypotonia Expressive language disorder
Congenital contractures Dimples
Hypertelorism Epicanthic folds Disorder of visual cortex
Low-set and posteriorly rotated ears
Micrognathia Cleft palate
ID Epilepsy Hypoplastic cerebellar vermis
Monozygotic twin, twin sister healthy
Tall stature Advanced bone age
Deep set eyes Hypotelorism Epicanthic folds Strabismus
Short nose Anteverted nares Tented upper lip
ID No speech Autism
Glypican-3 and PHF6 mutation analyses negative
ID Intractable epilepsy Tremor Myoclonias Distal spasticity
Small for Gestational Age
Downslanting palpebral fissures Strabismus
Exostosis (familial) Broad hallux Overriding toes Scoliosis
Downslanting palpebral fissures
Coarse hair Thick eyebrows Thick lips Malposition of teeth
Hip dis-placement Long thin bones
Epilepsy ID Alternating hemiplegia of childhood
Small for gestational age Prematurity Short stature
Severe myopia Coloboma of papillae Optic atrophy Nystagmus Strabismus
High palate Gum hypertrophy
Coarctation of aorta
ID Intractable epilepsy Hemiparesis (peri-ventricular leukomalacia)
Central blindness Nystagmus
ID Intractable epilepsy Hypotonia Distal spasticity
Vomiting Feeding difficulties
Dysmorphic malocclusion of teeth
Brain atrophy Epilepsy
Simian-crease Sinus pilonidalis
ID Intractable epilepsy Hypotonia Distal spasticity
Thin upper-lip Long philtrum Broad nasal bridge
ID Arnold Chiari malformation
DNA was extracted from blood samples according to standard protocols. Analysis by the Genome-wide human SNP array 6.0 was performed according to manufacturer protocols (Affymetrix, Santa Clara, CA, USA). In short; DNA was digested, ligated to adapters, and amplified by PCR. Samples were purified using magnetic beads and further fragmented and labelled with biotin. After hybridization arrays were washed and stained with streptavidin and anti-streptavidin antibodies and finally the arrays were scanned using the Affymetrix GeneChip scanner.
Data was extracted from the scanned image using the Genotyping console software V.3.0.2, creating a CEL file. Areas containing CNVs and allelic homozygosity were detected using the Hidden-Markow-Model. The resulting data was analyzed using the Chromosome Analysis Suite software V.1.0.
Data was extracted by comparison to a reference data set established from 90 Caucasian individuals, which had previously been analyzed using the SNP 6.0 array in the HapMap project (http://www.hapmap.org). As an additional in-house reference set, we used results of 54 individuals studied using the SNP 6.0 array, whereof 19 healthy normal relatives of the patients, and 35 unrelated patients with an unexplained developmental disorder. Sample identities were kept anonymous and the information was only used for reference purposes. These in-house reference sets were used to filter out polymorphic changes in the patient data studied here.
Selected CNVs of the patients were compared to a Finnish population cohort . This population cohort data consist of CNVs detected, using whole-genome SNP analysis, in 2163 healthy Finnish individuals with PennCNV . In the population data, low quality samples (N = 98) with Log R Ratio standard deviation of probe signal intensities > 0.35 or > 115 CNV calls were excluded. Only CNVs with three or more probes were included in the final population data. CNV calls of the study samples were clustered into CNV regions when individual CNVs overlapped by one or more base pairs.
Filtering relevant CNVs and potential UPDs
The first set of default filtering marked all duplications and deletions ≥0.7Kb and all allelic homozygosities ≥100Kb containing at least 10 markers to be included. This was based on the theoretical resolution of the array being 0.7Kb, in addition to information from the HapMap phase 1 study showing that approximately 70% of common haplotype blocks are ≤100Kb  . Allelic homozygosity was called by the analysis software where there was a stretch of homozygous SNPs in a chromosomal segment.
The second filtering was based on the comparison of all aberrations detected in the patients of this study (N = 35), an in-house patient reference set (N = 35) and an in-house normal reference set (N = 19) as well as the database of genomic variants (DGV) . Aberrations of one patient that were not present in any of the other groups (potentially “unique”) were further processed by studying their genetic content and association to diseases and traits, as stated in publications or OMIM, and whether these correlated to the patient’s phenotype. If this did not yield a candidate aberration, all aberrations of a patient were reviewed based on only the associated OMIM disease, despite the frequency of similar changes in the reference sets. The CNVs that were picked out as potential candidates were further compared to CNV data from 2,065 healthy Finnish individuals. Only those aberrations that were present in less than 50 individuals of the Finnish population cohort were initially considered as potentially pathogenic.
Validation of candidate aberrations
Only aberrations that were considered to potentially associate with patient’s phenotype were attempted validation.
Microsatellite marker analysis
Potential segmental UPDs were analyzed by microsatellite marker analysis (chr15: D15S204, D15S124; chr6: D6S468, D6S2418; chr11: D11S4140; chr17: D17S578, D17S1832, D17S1828).
The markers were selected based on their location, and on information that they are highly polymorphic in the Caucasian population. Fragments were labelled with a fluorescent HEX label, and separated on an Applied Biosystem 3730XL (Life Technologies, Carlsbad, CA, USA) capillary electrophoresis instrument, according to manufacturer recommendations. Genotypes were called using Applied Biosystems GeneMapper 3.7 software.
Results from microsatellite marker analysis
Associated OMIM disease (gene)
MIM #209900, Bardet-Biedl Syndrome (BBS4)
MIM #611092, Mental retardation (GRIK2)
MIM #270400, Smith-Lemli-Opitz syndrome (DHCR7)
MIM #201475, AcylCoA dehydrogenase deficiency (ACADVL)
We further attempted verification of four potential segmental UPDs by microsatellite marker analysis. In all the four cases we observed two distinct alleles with at least some of the more informative multiallelic markers, suggesting that the observed LOHs were most probably caused by the same allelic SNP haplotypes being inherited from both the parents (Table 2).
Regions of clustered allelic homozygosity
Appoximate range (Kb)
Frequency patients (n = 70)
Frequency normals (n = 19)
48 700–53 300
145 800–148 500
134 334–136 693
46 500–52 500
31 838–34 524
99 200–101 200
41 870–43 270
47 040–49 000
36 720–38 490
73 200–76 460
85 850–89 100
108 600–111 600
65 500–67 100
25 400–27 200
40 100–43 730
69 300–71 700
33 394–34 550
45 092–47 450
64 850–67 100
54 610–56 850
31 910–35 500
In our previous study of 150 patients with developmental disorders of unknown cause and a normal karyotype, we were able to identify a (potential) causative aberration in 18% of the patients, by using a 44 K or 244 K array CGH platform .
To determine whether, by increasing the resolution, any additional copy number changes or regions of UPD could be detected, we studied 35 patients with a normal array CGH result.
Allelic homozygosity is typically caused by linkage and co-segregation of certain blocks of DNA, termed haplotypes . In a small founder population, such as the Finnish population, the founder effect increases the likelihood that the parents will have the same haplotype, and is as such not a segmental UPD . True segmental UPD is typically due to a duplication in one chromosome and a reciprocal deletion in the other; or the fertilization of a disomic and monosomic gamete, somatic crossing over and subsequent trisomic rescue . If the genomic segment harbours a recessive mutation, which subsequent to UPD will be present in two copies (reduction to homozygosity), it causes a recessive disease. Equally relevant, the segment can be preferentially imprinted, causing complete silencing, which is the equivalent of a deletion. Such presentations of recessive syndromes that are inherited from one normal parent are known in some 40 patients .
We were interested to see whether the regions of allelic homozygosity detected by the SNP array were in fact segmental UPDs and associated with an autosomal recessive disease. We were, however, unable to confirm these results and thus the SNP array did not yield more molecular diagnoses in this study of developmental disorders of unknown cause. This may be due to the fact that all patients had previously been studied by another high-resolution array, with 8.9Kb (244 K), 13Kb (180 K), and 35Kb (44 K) theoretical resolutions. Although several new CNVs, previously undetected by the array CGH platform, as well as regions of homozygosity were detected, the pathogenic relevance of these changes were considered insignificant in correlation to the patient’s phenotype. It is, however, possible that changes dismissed in this study are pathogenic by means of spanning genomic segments that do not directly involve disease genes, but rather their regulatory elements.
Our results differ from previously published studies using similar research settings. Bernardini et al. (2010), using the SNP 6.0 array platform with a 75Kb cut-off value for detected CNVs, reported potentially pathogenic CNVs in 6% of patients with normal array CGH result (44 K) . Mannik et al. (2010), using another SNP array with a 50Kb resolution, reported a 23% detection rate in patients with a normal karyotype . Bernardini et al. and Mannik et al. had higher detection rates than this study; perhaps as their first-line of array analysis was, at least partly, done by a lower-resolution method (35Kb and 50Kb respectively) compared to the first-line of detection in this study (8,9Kb, 13Kb and 35Kb). Also, it is important to note that the statistical power is limited by the small size of our patient cohort, and thus results are not entirely comparable with Bernardini and Mannik’s.
UPDs have not been reported in either of the above mentioned studies. However, in a study of 117 patients with a normal karyotype analysed using the 250 K SNP array (Affymetrix, Santa Clara, CA, USA), pathogenic CNVs were detected in 18 patients, and potentially pathogenic segmental UPDs ≥5 Mb in 5, verified by microsatellite marker analysis . The presence of UPDs was also evaluated in another study of 120 patients, using a 500 K SNP array platform . In that study they were unable to verify UPD in any of 121 detected regions of homozygosity in 72 patients with developmental disorder of unknown cause. In addition, in a study of 100 patients with developmental disorder, using a 500 K SNP array, two patients were found to have UPD, the clinical significance of which remained unclear . Thus, UPDs are detectable using SNP arrays, but their clinical significance is difficult to interpret.
Although there is a clear added value of high-resolution arrays in various fields of genetics, it seems that there is a limit to how much the yield can be increased by increasing the theoretical resolution of the analysis platform. Despite the fact that the SNP array has increased probe spacing compared to the 44 K, 180 K, and 244 K array, and is able to detect more CNVs and regions of homozygosity, interpretation of the vast amount of data and pinpointing of pathogenic changes is difficult. One benefit of using a SNP based platform is the possibility to detect UPDs; however these are relatively rare findings.
This study had a limited number of patients, and so it can only be said that for this study group the optimal yield was conceived when using a resolution of approximately 9Kb . Increasing the resolution beyond that did not confer more diagnoses. It must be emphasized, however, that a larger patient cohort needs to be studied in order to draw final conclusions on the added value of an ultra-high resolution array compared to others. Furthermore, as several reports have shown, some pathogenic aberrations span only a few exons and for detecting such small changes the sensitivity of the SNP 6.0 platform is adequate . It is, however a challenge to filter results correctly and so for diagnostic purposes the choice of platform needs to be carefully considered. Patients with developmental disorders of unknown cause and normal array results may also harbour such small genomic changes (i.e. mutations and unbalanced rearrangements) that are difficult to interpret using microarrays and would require higher resolution methods, such as whole-exome sequencing. Interestingly, a recent study suggests that 80% of patients with a developmental disorder of unknown cause and normal array results can be diagnosed using whole-exome sequencing . Only the future can tell.
Availability of supporting data
The data set supporting the results of this article is available in the CanGEM repository, http://www.cangem.org/browse.php.
We thank all the participating patients and their families. A thanks to Marketta Dalla Valle for her contribution of clinical information. The staff from the Genotyping Facilities at the Wellcome Trust Sanger Institute is acknowledged for genotyping of the Health 2000 study sample. This study was kindly supported by Rinnekoti Research Foundation, Medicinska Understödsföreningen Liv och Hälsa rf., and The Helsinki and Uusimaa Hospital District State Appropriations. K.K. was supported by the Orion-Farmos Research Foundation and the Academy of Finland (grant no. 125973).
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