Additional file 1 of Quantitative thresholds for variant enrichment in 13,845 cases: improving pathogenicity classification in genetic hearing loss

Additional file 1: Table S1. List of 115 SNVs and three CNVs in SNPscan assay. Table S2. 157 hearing loss related genes included in the CDGC-HL panel. Table S3. 9,050 variants included in this study. Table S4. Allele frequency thresholds for variants could reach p-value

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Bibliographische Detailangaben
Hauptverfasser:	Liu, Sihan, Zhong, Mingjun, Huang, Yu, Zhang, Qian, Chen, Ting, Xu, Xiaofei, Peng, Wan, Wang, Xiaolu, Feng, Xiaoshu, Kang, Lu, Lu, Yu, Cheng, Jing, Bu, Fengxiao, Yuan, Huijun
Format:	Dataset
Sprache:	eng
Schlagworte:	FOS: Biological sciences Genetics
Online-Zugang:	Volltext bestellen
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Beschreibung
Zusammenfassung:	Additional file 1: Table S1. List of 115 SNVs and three CNVs in SNPscan assay. Table S2. 157 hearing loss related genes included in the CDGC-HL panel. Table S3. 9,050 variants included in this study. Table S4. Allele frequency thresholds for variants could reach p-value
DOI:	10.6084/m9.figshare.24864106