Variant Details

Variant: esv3627845

Internal ID

7014670

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:117121067..117121771	hg38	UCSC Ensembl
Inner	chr11:117121067..117121771	hg38	UCSC Ensembl
Outer	chr11:117120680..117122179	hg38	UCSC Ensembl
	chr11:116991783..116992487	hg19	UCSC Ensembl
Inner	chr11:116991783..116992487	hg19	UCSC Ensembl
Outer	chr11:116991396..116992895	hg19	UCSC Ensembl

Cytoband

11q23.3

Allele length

Assembly	Allele length
hg38	705
hg19	705

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv14292640, essv14292602, essv14292629, essv14292583, essv14292615, essv14292599, essv14292585, essv14292625, essv14292649, essv14292637, essv14292582, essv14292622, essv14292633, essv14292643, essv14292592, essv14292646, essv14292612, essv14292584, essv14292609, essv14292650, essv14292620, essv14292603, essv14292631, essv14292658, essv14292611, essv14292617, essv14292654, essv14292619, essv14292621, essv14292630, essv14292601, essv14292588, essv14292636, essv14292600, essv14292648, essv14292624, essv14292586, essv14292604, essv14292638, essv14292616, essv14292642, essv14292627, essv14292639, essv14292623, essv14292656, essv14292608, essv14292610, essv14292614, essv14292655, essv14292598, essv14292607, essv14292651, essv14292659, essv14292587, essv14292589, essv14292593, essv14292618, essv14292626, essv14292645, essv14292641, essv14292657, essv14292652, essv14292613, essv14292597, essv14292653, essv14292635, essv14292594, essv14292660, essv14292591, essv14292647, essv14292590, essv14292644, essv14292628, essv14292634, essv14292632, essv14292595, essv14292605, essv14292596, essv14292606

Samples

HG00626, HG00881, HG00592, HG02072, HG00608, NA18621, HG01031, HG02035, HG02360, HG02382, HG02394, HG00449, HG00654, HG00663, NA18563, NA18940, NA18550, HG02153, HG02185, NA18597, HG02140, HG00689, HG00674, HG00458, HG01843, NA18618, HG02130, HG02085, HG01859, HG02131, HG02389, NA18748, HG02082, NA18990, HG02073, NA18640, HG00530, HG01851, HG01841, HG01797, HG01595, HG02025, HG01857, HG01864, HG00701, HG00598, NA18637, HG02522, HG01808, NA18548, NA18537, HG02364, HG00844, NA18946, NA19001, NA18553, HG00463, HG00864, NA18593, HG01596, HG00445, HG02696, NA18950, HG02064, HG00638, HG02137, HG02371, HG00707, HG00446, HG02367, HG01868, NA18987, HG01817, NA18552, NA18983, HG02353, NA19011, HG01869, HG02406

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3627845

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	79
Observed Complex	0
Frequency	n/a