Skip to main content

Advertisement

Springer Nature is making SARS-CoV-2 and COVID-19 research free. View research | View latest news | Sign up for updates

Table 2 Size of CNVs in breast cancer cases and controls across the whole genome, and overlapping genomic features

From: Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry

CNV type Mean size of CNVs (kb) Difference in means (kb) Case/control ratio P value
Cases (n = 200) Controls (n = 293) Case - controls 95% CI
All 59.4 65.7 -6.3 -10.1, -2.5 0.90 0.001
Deletions 42.9 42.7 0.2 -3.0, 3.4 1.00 0.89
Gains 10.1 10.0 0.1 -7.7, 10.3 1.01 0.77
  1. CNV copy number variation