Additional file 1: Table S1. of Assessing the reproducibility of exome copy number variations predictions
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Lists all the IDs used in this study. Table S2 gives details of independent dataset analysis. Tables S3 and S4 give details of size and capture analyses. Table S5 lists ClinSeqÂŽ CNVs identified from SNP chips used in this study. Table S6 lists the summary of CNV sizes for 300 ClinSeq run at base pair and exon resolution. Table S7 lists SNP array CNV calls used for 300 ClinSeq samples. (XLSX 57 kb)
创建时间：
2023-06-28
