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Fig. 3 | BMC Medical Genetics

Fig. 3

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

Fig. 3

Linked-read sequencing data for two pHGG patients at the BTNL8-BTNL3 locus. a Homozygous BTNL8-BTNL3 deletion in the tumor profile of patient 6 (G641). b Homozygous deletion in the germline of patient 6 (G641B). c Heterozygous BTNL8-BTNL3 deletion in the tumor profile of patient 1 (SM2932). d Heterozygous deletion in the germline of patient 1(SM2819)

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