Additional file 3: of Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases

Authors :: Dharmadhikari, Avinash
Rajarshi Ghosh
Yuan, Bo
Pengfei Liu
Hongzheng Dai
Masri, Sami
Scull, Jennifer
Posey, Jennifer
Jiang, Allen
Weimin He
Vetrini, Francesco
Braxton, Alicia
Ward, Patricia
Chiang, Theodore
Chunjing Qu
Gu, Shen
Shaw, Chad
Smith, Janice
Lalani, Seema
Stankiewicz, Pawel
Sau-Wai Cheung
Bacino, Carlos
Ankita Patel
Breman, Amy
Wang, Xia
Linyan Meng
Xiao, Rui
Xia, Fan
Muzny, Donna
Gibbs, Richard
Beaudet, Arthur
Eng, Christine
Lupski, James
Yaping Yang
Weimin Bi
Publisher :: figshare
Abstract: Supplementary Table S1. Correlation of PCNV findings from CMA and the QC array in 496 ES cases (DOCX 44 kb)

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