Fig. 3From: Ancestry and frequency of genetic variants in the general population are confounders in the characterization of germline variants linked to cancerLinked-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)Back to article page