Additional file 5: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
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Types and number of variants detected (exome- and CAGP-wide) before and after variant filtration in each BC patient and control. (XLSX 32 kb)
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figshare创建时间：
2019-04-05
