Fig. 1From: Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registryPutative copy number variation (CNV) calls overlapping known cancer susceptibility genes in five cases of early-onset breast cancer. UCSC Genome Browser screenshots (NCBI36/hg18) show the location of the CNVs (solid red rectangles) in relation to each gene. RefSeq reference sequenceBack to article page