Whole Exome Sequence of 184 Individuals with 22q11.2 Deletion Syndrome

dbGaP FAQdbGaP Access Request Video Tutorial

Platforms

dbGaP

View in dbGaP

phs000987.v1.p1

APIs

Consent Codes

GRU-IRB

Focus / Diseases

DiGeorge Syndrome

Study Design

Case Set

Data Types

SNP/CNV Genotypes (NGS), WXS

Subjects

184