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Figure 4 | BMC Medical Genetics

Figure 4

From: Identification of a rare 17p13.3 duplication including the BHLHA9 and YWHAEgenes in a family with developmental delay and behavioural problems

Figure 4

Schematic representation of five 17p13.3 duplications in relation to gene content. Enlargement of band p13.3 of chromosome 17. For each individual, the solid lines (grey shading) below the map represent duplicated regions and nucleotide positions are indicated according to UCSC Genome Browser Build 36.1 2009 (nucleotide positions of Bi cases 1 and 2 and Bruno cases 9 and 11 were converted from Hg18; nucleotide position of Bi case 1 was deduced (not indicated in the report). The dotted lines restrict the minimal critical region of overlap for 17p13.3 microduplications in the five cases.

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