Variant Details

Variant: esv3616916

Internal ID

7003802

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr8:38077573..38080769	hg38	UCSC Ensembl
Inner	chr8:38077573..38080769	hg38	UCSC Ensembl
Outer	chr8:38077278..38081132	hg38	UCSC Ensembl
	chr8:37935091..37938287	hg19	UCSC Ensembl
Inner	chr8:37935091..37938287	hg19	UCSC Ensembl
Outer	chr8:37934796..37938650	hg19	UCSC Ensembl

Cytoband

8p11.23

Allele length

Assembly	Allele length
hg38	3197
hg19	3197

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv13169091, essv13169032, essv13169130, essv13169047, essv13169127, essv13169057, essv13169133, essv13169054, essv13169028, essv13169067, essv13169105, essv13169037, essv13169040, essv13169099, essv13169131, essv13169033, essv13169066, essv13169036, essv13169059, essv13169041, essv13169121, essv13169063, essv13169113, essv13169107, essv13169050, essv13169038, essv13169073, essv13169110, essv13169116, essv13169034, essv13169035, essv13169075, essv13169129, essv13169132, essv13169071, essv13169058, essv13169080, essv13169052, essv13169026, essv13169128, essv13169115, essv13169089, essv13169056, essv13169046, essv13169101, essv13169051, essv13169083, essv13169078, essv13169043, essv13169122, essv13169062, essv13169100, essv13169103, essv13169072, essv13169086, essv13169092, essv13169120, essv13169085, essv13169022, essv13169030, essv13169068, essv13169084, essv13169098, essv13169119, essv13169076, essv13169061, essv13169053, essv13169049, essv13169109, essv13169112, essv13169090, essv13169024, essv13169111, essv13169048, essv13169031, essv13169065, essv13169123, essv13169042, essv13169082, essv13169096, essv13169117, essv13169074, essv13169069, essv13169104, essv13169055, essv13169126, essv13169106, essv13169125, essv13169087, essv13169114, essv13169124, essv13169095, essv13169064, essv13169102, essv13169093, essv13169070, essv13169029, essv13169077, essv13169094, essv13169118, essv13169060, essv13169108, essv13169039, essv13169027, essv13169081, essv13169044, essv13169025, essv13169079, essv13169021, essv13169088, essv13169045, essv13169097, essv13169023

Samples

NA21111, NA19397, NA21089, NA20877, NA11829, HG04222, NA21099, HG02784, NA21100, NA19734, HG03941, HG04018, HG03018, NA21137, NA20863, NA19443, HG03944, HG03679, HG03645, HG03016, HG03796, HG03705, HG04022, NA20850, HG01997, NA21130, NA20769, HG03736, HG03663, HG03911, HG02603, HG03917, HG03793, NA12156, HG03788, HG03888, NA21107, NA19036, HG03744, NA20884, NA21114, HG03585, HG03784, HG01524, NA21106, NA20904, HG03697, HG00629, HG03685, HG01187, NA19056, HG04225, NA19006, HG04062, NA21119, HG03786, HG02775, HG02522, NA21118, HG03756, NA12234, HG03823, HG03021, HG01777, HG03871, HG03730, NA20901, HG00844, NA20859, HG04155, NA20881, HG03631, HG03643, HG04189, HG02724, HG02725, HG03672, HG03752, HG00463, HG04159, HG03991, NA21142, NA18646, NA18608, HG01363, NA20799, HG03848, HG02684, HG01678, NA21123, HG03869, HG03488, NA20902, NA19439, HG03012, HG03779, HG00125, HG02700, NA18971, HG04140, HG04015, HG03789, NA20849, HG03022, NA21101, HG03894, HG03872, HG02028, HG02778, HG03985, NA20772, HG03989, NA18997

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3616916

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	113
Observed Complex	0
Frequency	n/a