ID   GM10606
AC   CVCL_5P21
DR   CLO; CLO_0024282
DR   Coriell; GM10606
DR   Wikidata; Q54844549
RX   CelloPub=CLPUB00447;
RX   PubMed=23665875;
CC   Karyotypic information: 69,XXX,dup(20)(pter->q13.2::q11.2->qter).arr 3q21.3(129973405-130112434)x3,8p23.1(7242445-7825360)x1,20q11.21q13.2(29298697-54338231)x3 (Coriell=GM10606).
CC   Omics: CNV analysis.
CC   Derived from site: In situ; Whole fetus; UBERON=UBERON_0000323.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C85204; Triploidy syndrome
DI   ORDO; Orphanet_3376; Triploidy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   Fetus
CA   Finite cell line
DT   Created: 23-02-16; Last updated: 29-06-23; Version: 9
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RX   CelloPub=CLPUB00447;
RA   Mulivor R.A., Suchy S.F.;
RT   "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 16th edition. October 1992.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992).
//
RX   PubMed=23665875; DOI=10.1534/g3.113.006577;
RA   Tang Z.-Y., Berlin D.S., Toji L.H., Toruner G.A., Beiswanger C.M.,
RA   Kulkarni S., Martin C.L., Emanuel B.S., Christman M., Gerry N.P.;
RT   "A dynamic database of microarray-characterized cell lines with
RT   various cytogenetic and genomic backgrounds.";
RL   G3 (Bethesda) 3:1143-1149(2013).
//