Additional file 3: Table S2. of Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability
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资源简介：
Primers for verification - All primer sequences used for SNV, CNV and SV verification. (XLSX 18 kb)
验证用引物 —— 本数据集包含用于单核苷酸变异（Single Nucleotide Variant, SNV）、拷贝数变异（Copy Number Variant, CNV）及结构变异（Structural Variant, SV）验证的全部引物序列。（XLSX 18 kb）
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Figshare
创建时间：
2017-12-18
