Whole Genome Sequencing of Two 22q11DS Trios
Demographics (1)
- Sex - Gender of participant (phv00222265.v1.p1)
Disease Events (4)
- AFFECTION_STATUS - 22q11DS case control status of the subject (phv00222253.v1.p1)
- deletion_status - Subject has 22q11.2 deletion (phv00222266.v1.p1)
- systemic_juvenile_rheumatoid_arthritis - Juvenile rheumatoid arthritis status (phv00222269.v1.p1)
- tetralogy_of_fallot - Tetralogy of Fallot status (phv00222267.v1.p1)
Mental Health (1)
- other_specified_schizophrenia_spectrum - Other specified schizophrenia spectrum and other psychotic disorder (phv00222268.v1.p1)
Other (21)
- ANALYTE_TYPE - Analyte Type (phv00222273.v1.p1)
- BODY_SITE - Body site where sample was collected (phv00222271.v1.p1)
- CELL_LINE - Is DNA from cell line (phv00222272.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00222250.v1.p1)
- FAMILY_ID - Family ID (phv00222254.v1.p1)
- FATHER - Father's Subject ID (phv00222257.v1.p1)
- MOTHER - Mother's Subject ID (phv00222256.v1.p1)
- PROBAND - Is subject a 22q11DS proband (phv00222275.v1.p1)
- SAMPLE_ID - De-identified Sample ID (phv00222270.v1.p1)
- SAMPLE_ID - Sample ID (phv00222260.v1.p1)
- SAMPLE_SOURCE - Source repository where samples originate (phv00222261.v1.p1)
- SAMPLE_USE - Sample use. Seq_DNA_SNP: SNP genotypes derived from sequence data; Seq_DNA_WholeGenome: Whole genome sequencing (phv00222263.v1.p1)
- SEQUENCING_CENTER - Name of the center which conducted sequencing (phv00222274.v1.p1)
- SEX - Sex (phv00222258.v1.p1)
- SOURCE_SAMPLE_ID - Sample ID used in the Source Repository (phv00222262.v1.p1)
- SOURCE_SUBJECT_ID - Subject ID used in the Source Repository (phv00222252.v1.p1)
- SUBJECT_ID - De-identified Subject ID (phv00222264.v1.p1)
- SUBJECT_ID - Subject ID (phv00222249.v1.p1)
- SUBJECT_ID - Unique Subject ID (phv00222255.v1.p1)
- SUBJECT_ID - Subject ID (phv00222259.v1.p1)
- SUBJECT_SOURCE - Source repository where subjects originate (phv00222251.v1.p1)