Additional file 3: Table S2. of Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry

Taqman assays used for CNV assessment at 7 gene loci. Table S3. Cancer-predisposing genes disrupted by rare CNVs. Table S4. Results of Taqman assays carried across 7 gene loci. (DOCX 18 kb