Fig. 3: Associations with duplications at the 17p13.3 locus.
From: Rare germline copy number variants (CNVs) and breast cancer risk
Log odds ratios for individual probes from Oncoarray and iCOGs are shown at the top in green. Genes from the Ensembl browser are shown in the next row, followed by structural variants identified by the 1000 Genomes Project with duplications in blue and deletions in red.
