ID   DD1620
AC   CVCL_9G76
DR   ECACC; 93112927
DR   Wikidata; Q54829888
CC   Part of: ECACC chromosomal abnormality collection.
CC   Derived from site: In situ; Umbilical cord; UBERON=UBERON_0002331.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C2989; 22q11.2 deletion syndrome
DI   ORDO; Orphanet_567; 22q11.2 deletion syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   4D
CA   Finite cell line
DT   Created: 23-02-16; Last updated: 29-06-23; Version: 7
//