ID GM20785 AC CVCL_P636 DR CLO; CLO_0028884 DR ArrayExpress; E-GEUV-1 DR ArrayExpress; E-GEUV-2 DR ArrayExpress; E-GEUV-3 DR BioSample; SAMN00001298 DR Coriell; GM20785 DR GEO; GSM650343 DR GEO; GSM1720462 DR IGSR; NA20785 DR Wikidata; Q54851281 RX PubMed=21397061; RX PubMed=24037378; RX PubMed=27617755; CC Part of: International Genome Sample Resource (1000 genomes project) cell lines. CC Population: Caucasian; Toscani in Italia (TSI). CC Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV). CC Omics: CNV analysis. CC Omics: Genome sequenced. CC Omics: Transcriptome analysis by RNAseq. CC Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. OX NCBI_TaxID=9606; ! Homo sapiens (Human) SX Male AG Age unspecified CA Transformed cell line DT Created: 05-11-13; Last updated: 29-06-23; Version: 15 // RX PubMed=21397061; DOI=10.1016/j.ajhg.2011.02.004; PMCID=PMC3059424; RA Campbell C.D., Sampas N., Tsalenko A., Sudmant P.H., Kidd J.M., RA Malig M., Vu T.H., Vives L., Tsang P., Bruhn L., Eichler E.E.; RT "Population-genetic properties of differentiated human copy-number RT polymorphisms."; RL Am. J. Hum. Genet. 88:317-332(2011). // RX PubMed=24037378; DOI=10.1038/nature12531; PMCID=PMC3918453; RA Lappalainen T., Sammeth M., Friedlander M.R., 't Hoen P.A.C., RA Monlong J., Rivas M.A., Gonzalez-Porta M., Kurbatova N., Griebel T., RA Ferreira P.G., Barann M., Wieland T., Greger L., van Iterson M., RA Almlof J.C., Ribeca P., Pulyakhina I., Esser D., Giger T., Tikhonov A., RA Sultan M., Bertier G., MacArthur D.G., Lek M., Lizano E., RA Buermans H.P.J., Padioleau I., Schwarzmayr T., Karlberg O., Ongen H., RA Kilpinen H., Beltran S., Gut M., Kahlem K., Amstislavskiy V., RA Stegle O., Pirinen M., Montgomery S.B., Donnelly P., McCarthy M.I., RA Flicek P., Strom T.-M., Lehrach H., Schreiber S., Sudbrak R., RA Carracedo A., Antonarakis S.E., Hasler R., Syvanen A.-C., RA van Ommen G.-J.B., Brazma A., Meitinger T., Rosenstiel P., Guigo R., RA Gut I.G., Estivill X., Dermitzakis E.T.; RG Geuvadis Consortium; RT "Transcriptome and genome sequencing uncovers functional variation in RT humans."; RL Nature 501:506-511(2013). // RX PubMed=27617755; DOI=10.1038/srep32406; PMCID=PMC5019111; RA Ferreira P.G., Oti M., Barann M., Wieland T., Ezquina S., RA Friedlander M.R., Rivas M.A., Esteve-Codina A., Rosenstiel P., RA Strom T.-M., Lappalainen T., Guigo R., Sammeth M.; RG Geuvadis Consortium; RT "Sequence variation between 462 human individuals fine-tunes RT functional sites of RNA processing."; RL Sci. Rep. 6:32406-32406(2016). //