ID   DD1641
AC   CVCL_9G83
DR   ECACC; 93120316
DR   Wikidata; Q54829896
CC   Part of: ECACC chromosomal abnormality collection.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
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
//