ID HG00362 AC CVCL_P850 DR ArrayExpress; E-GEUV-1 DR ArrayExpress; E-GEUV-2 DR ArrayExpress; E-GEUV-3 DR BioSamples; SAME124537 DR Coriell; HG00362 DR GEO; GSM649678 DR GEO; GSM1718235 DR IGSR; HG00362 DR Wikidata; Q54883505 RX PubMed=21397061; RX PubMed=24037378; RX PubMed=27617755; CC Part of: International Genome Sample Resource (1000 genomes project) cell lines. CC Population: Caucasian; Finnish in Finland (FIN). CC Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV). CC Omics: Genomics; Whole genome sequencing. CC Omics: Transcriptomics; RNAseq. CC Omics: Variations; CNV analysis. CC Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. OX NCBI_TaxID=9606; ! Homo sapiens (Human) SX Female AG Age unspecified CA Transformed cell line DT Created: 05-11-13; Last updated: 10-04-25; Version: 16 // 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). //