Identification of Modifiers of 22q11.2 Deletion Syndrome in Whole Genome Sequence - CIDR
Demographics (2)
- SEX - Biological sex (phv00503655.v1.p1)
- SEX - Biological sex (phv00503660.v1.p1)
Race and Ethnicity (1)
- RACE - Self-reported race (phv00503665.v1.p1)
Other (20)
- AFFECTON_STATUS - Whether or not the subject has congenital heart disease (phv00503664.v1.p1)
- ANALYTE_TYPE - Analyte type (phv00503670.v1.p1)
- BODY_SITE - Body site where sample was taken (phv00503669.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00503654.v1.p1)
- DELETION_SIZE - The type of hemizygous deletion in 22q11.2 region that each patient has (phv00503666.v1.p1)
- FAMILY_ID - Family ID (phv00503656.v1.p1)
- FATHER - Father's Subject ID (phv00503658.v1.p1)
- IS_TUMOR - The tumor status of the sample (phv00503671.v1.p1)
- MOTHER - Mother's Subject ID (phv00503659.v1.p1)
- SAMPLE_ID - De-identified Sample ID (phv00503668.v1.p1)
- SAMPLE_ID - Sample ID (phv00503662.v1.p1)
- SHIPMENT_SITE - The site where the sample comes from (phv00503667.v1.p1)
- SOURCE_SUBJECT_ID - Overlapping subject's ID in phs000987 (phv00508369.v1.p1)
- SOURCE_SUBJECT_ID2 - Overlapping subject's ID in phs001339 (phv00529988.v1.p1)
- SUBJECT_ID - Subject ID (phv00503653.v1.p1)
- SUBJECT_ID - Subject ID (phv00503657.v1.p1)
- SUBJECT_ID - Subject ID (phv00503663.v1.p1)
- SUBJECT_ID - Subject ID (phv00503661.v1.p1)
- SUBJECT_SOURCE - Repository/Cohort designation of subjects who also participated in prior dbGaP study (phv00508368.v1.p1)
- SUBJECT_SOURCE2 - Repository/Cohort designation of subjects who participated in an additional prior dbGaP study (phv00529987.v1.p1)