Additional file 8: Table S6. of Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability
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Raw data for SNVs detected across all patients by Mendelian Inheritance Pattern filtering â all SNVs detected per trio, organized as one trio per sheet, using the Mendelian inheritance filtering. Sheet 1 gives the legend. All SNVs are annotated, including CADD and RVIS scores. (XLSX 57 kb)
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Linlea Armstrong
创建时间：
2017-05-25
