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Fig. 1 | BMC Medical Genetics

Fig. 1

From: Ancestry and frequency of genetic variants in the general population are confounders in the characterization of germline variants linked to cancer

Fig. 1

Linked-read sequencing data for two pHGG patients at the NEGR1 locus. a. Homozygous NEGR1 deletion in the tumor profile of patient 6 (G641). b. Homozygous deletion in the germline of patient 6 (G641B). c. Heterozygous NEGR1 deletion in the tumor profile of patient 1 (SM2932). d. Heterozygous deletion in the germline of patient 1 (SM2819). In all panels, linked-reads are organized in haplotype blocks. Each haplotype is color-coded (green/yellow or pink/purple). Unassigned linked-reads are shown in back/gray at the bottom of each panel

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BMC Medical Genetics

ISSN: 1471-2350

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