Whole Exome Sequence of Hearing Loss Family
Demographics (2)
- Sex - Gender of participant (phv00252647.v1.p1)
- SEX - Sex (phv00252640.v1.p1)
Disease Events (1)
- AFFECTION_STATUS - Deafness case control status of the subject (phv00252635.v1.p1)
Race and Ethnicity (2)
- ethnicity - Ethnicity of participant (phv00252649.v1.p1)
- race - Race of participant (phv00252648.v1.p1)
Other (21)
- ANALYTE_TYPE - Analyte type (phv00252654.v1.p1)
- BODY_SITE - Body site where sample was taken (phv00252652.v1.p1)
- CELL_LINE - DNA derived from cell line (phv00252653.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00252632.v1.p1)
- deafness - Bilateral deafness status (phv00252650.v1.p1)
- FAMILY_ID - Family ID (phv00252636.v1.p1)
- FATHER - Father ID (phv00252639.v1.p1)
- MOTHER - Mother ID (phv00252638.v1.p1)
- PROBAND - Subject with deafness (phv00252656.v1.p1)
- SAMPLE_ID - De-identified Sample ID (phv00252651.v1.p1)
- SAMPLE_ID - Sample ID (phv00252642.v1.p1)
- SAMPLE_SOURCE - Source repository where samples originate (phv00252643.v1.p1)
- SAMPLE_USE - Sample Use (phv00252645.v1.p1)
- SEQUENCING_CENTER - Name of the center which conducted sequencing (phv00252655.v1.p1)
- SOURCE_SAMPLE_ID - Sample ID used in the Source Repository (phv00252644.v1.p1)
- SOURCE_SUBJECT_ID - Subject ID used in the Source Repository (phv00252634.v1.p1)
- SUBJECT_ID - Subject ID (phv00252631.v1.p1)
- SUBJECT_ID - Unique Subject ID (phv00252637.v1.p1)
- SUBJECT_ID - Subject ID (phv00252641.v1.p1)
- SUBJECT_ID - De-identified Subject ID (phv00252646.v1.p1)
- SUBJECT_SOURCE - Source repository where subjects originate (phv00252633.v1.p1)