Additional file 9 of Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes
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https://springernature.figshare.com/articles/dataset/Additional_file_9_of_Integration_of_genetic_transcriptomic_and_clinical_data_provides_insight_into_16p11_2_and_22q11_2_CNV_genes/16907218/1
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Additional file 9: Table S8. Traits over-represented in CNV carriers. The four categories of CNV carrier – 16p11.2 duplication, 16p11.2 deletion, 22q11.2 duplication, 22q11.2 deletion – were tested separately. The results for all clinical traits tested are provided. The number of cases and controls for each trait is given, as well as whether the p-value meets either Bonferroni or FDR correction. Traits in bold were represented in over 5% of carriers.
提供机构：
Zhong, Xue; Zhou, Dan; Weiss, Lauren A.; Cox, Nancy J.; Miller-Fleming, Tyne W.; Vysotskiy, Mikhail
创建时间：
2021-10-30
