ID   GM08206
AC   CVCL_1N82
DR   CLO; CLO_0010129
DR   Coriell; GM08206
DR   Wikidata; Q54843100
RX   PubMed=23665875;
CC   Population: Caucasian.
CC   Karyotypic information: 46,XY.arr(1-22)x2,(XY)x1 (Coriell=GM08206).
CC   Omics: Variations; CNV analysis.
CC   Derived from site: In situ; Liver; UBERON=UBERON_0002107.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C34415; Beckwith-Wiedemann syndrome
DI   NCIt; C3728; Hepatoblastoma
DI   ORDO; Orphanet_116; Beckwith-Wiedemann syndrome
DI   ORDO; Orphanet_449; Hepatoblastoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   7M
CA   Finite cell line
DT   Created: 08-07-15; Last updated: 10-04-25; Version: 10
//
RX   PubMed=23665875; DOI=10.1534/g3.113.006577; PMCID=PMC3704242;
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).
//