characteristics.text: SAMN04041300
characteristics.characteristic: External Id
characteristics.text: dbGaP
characteristics.characteristic: INSDC center name
characteristics.text: 2015-09-09T03:05:29.130Z
characteristics.characteristic: INSDC first public
characteristics.text: 2025-08-10T20:48:48.420Z
characteristics.characteristic: INSDC last update
characteristics.text: SRS1379614
characteristics.characteristic: INSDC secondary accession
characteristics.text: live
characteristics.characteristic: INSDC status
characteristics.text: Generic
characteristics.characteristic: NCBI submission model
characteristics.text: Generic.1.0
characteristics.characteristic: NCBI submission package
characteristics.text: SRS1379614
characteristics.characteristic: SRA accession
characteristics.text: DNA
characteristics.characteristic: analyte type
characteristics.text: NHLBI_CardiovascularAnomalies_22q11DS
characteristics.characteristic: biospecimen repository
characteristics.text: 42344
characteristics.characteristic: biospecimen repository sample id
characteristics.text: blood
characteristics.ontologyTerms: http://purl.obolibrary.org/obo/UBERON_0000178
characteristics.characteristic: body site
characteristics.text: phs000987
characteristics.characteristic: gap_accession
characteristics.text: 1
characteristics.characteristic: gap_consent_code
characteristics.text: GRU-IRB
characteristics.characteristic: gap_consent_short_name
characteristics.text: 1749658
characteristics.characteristic: gap_sample_id
characteristics.text: 1336785
characteristics.characteristic: gap_subject_id
characteristics.text: SNP/CNV Genotypes (NGS)
characteristics.characteristic: molecular data type
characteristics.text: Homo sapiens
characteristics.ontologyTerms: http://purl.obolibrary.org/obo/NCBITaxon_9606
characteristics.characteristic: organism
characteristics.text: male
characteristics.ontologyTerms: http://purl.obolibrary.org/obo/PATO_0000384
characteristics.characteristic: sex
characteristics.text: Case Set
characteristics.characteristic: study design
characteristics.text: DiGeorge Syndrome
characteristics.ontologyTerms: http://www.orpha.net/ORDO/Orphanet_567
characteristics.characteristic: study disease
characteristics.text: Whole Exome Sequence of 184 Individuals with 22q11.2 Deletion Syndrome
characteristics.characteristic: study name
characteristics.text: Yes
characteristics.characteristic: subject is affected
characteristics.text: 42344
characteristics.characteristic: submitted sample id
characteristics.text: CH04-144
characteristics.characteristic: submitted subject id
characteristics.text: NHLBI_CardiovascularAnomalies_22q11DS
characteristics.characteristic: submitter handle
characteristics.text: DNA sample from blood of a human male participant in the dbGaP study Whole Exome Sequence of 184 Individuals with 22q11.2 Deletion Syndrome
characteristics.characteristic: title