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Table 2 CNV association study samples

From: Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss

Phenotype Total Gender Ethnicity
Female Male Caucasian Mexican East Asian Native American African American African American-Caucasian Caucasian-East Asian Middle Eastern
Affected 150 65 85 44 59 27 6 4 6 4 0
Unaffected 157 79 78 132 16 5 0 2 0 2 1
  1. Affected individuals were recruited at Stanford University under IRB approval. Unaffected individuals matched for sex, age, and ethnicity were collected under IRB approval at Stanford University (n = 31), Mount Sinai University (n = 88) and Yale University (n = 38) using identical selection criteria. Ethnicity was determined using Principal Components Analysis with the Human Genome Diversity Panel.