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. Author manuscript; available in PMC: 2020 Jul 1.
Published in final edited form as: Cancer Epidemiol Biomarkers Prev. 2019 Apr 4;28(7):1117–1126. doi: 10.1158/1055-9965.EPI-18-0833

Figure 1. Common CNV regions generated from two SNP-array data sets.

Figure 1.

Copy number variation regions (CNVR) were compared between 2.5M and 610k array sets. Bar charts depict the number of deletion and duplication CNVRs that were common in each set. The overlap between sets is denoted by stacked bars.