Variant Details

Variant: esv2676468

Internal ID

9942573

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr1:212908674..212912780	hg38	UCSC Ensembl
Outer	chr1:212908303..212913150	hg38	UCSC Ensembl
Inner	chr1:213082016..213086122	hg19	UCSC Ensembl
Outer	chr1:213081645..213086492	hg19	UCSC Ensembl

Cytoband

1q32.3

Allele length

Assembly	Allele length
hg38	4848
hg19	4848

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6249143, essv5421048, essv5724527, essv6251199, essv5804339, essv5902843, essv6334025, essv6156957, essv5505195, essv6145410, essv6383716, essv5783533, essv6348836, essv6121536, essv5651051, essv5436844, essv5805597, essv6047455, essv6112489, essv5750782, essv6445373, essv6568250, essv5431955, essv5877539, essv5468121, essv5865127, essv5860741, essv5604336, essv6393324, essv6248114, essv5993951, essv5474858, essv5902231, essv6401546, essv5917386, essv5783645, essv6029673, essv5639375, essv5956727, essv5482527, essv5815792, essv6322815, essv5484526, essv6241162, essv5950261, essv5434012, essv6247805, essv6137221, essv5817145, essv6323833, essv6408610, essv6286003, essv6347298, essv6518807, essv6137487, essv6525518, essv6015180, essv5477823, essv6024458, essv6585642, essv5926683, essv5959500, essv6344005, essv5967910, essv5679979, essv5929287, essv5872364, essv6208816, essv6565070, essv5999329, essv6195868, essv5859819, essv5796973, essv5680067, essv6300340, essv6095313, essv6121661, essv6200010, essv5493504, essv5646743, essv5608563, essv5858054, essv5931316, essv5729476

Samples

HG00626, HG00403, HG00650, HG00542, HG00442, HG00592, HG00536, HG00608, HG00671, HG00559, HG00524, HG00699, HG00566, HG00449, HG00654, HG00693, HG00589, HG00501, HG00702, HG00689, HG00448, HG00634, HG00610, HG00512, HG00683, HG00534, HG00422, HG00705, HG00427, HG00530, HG00419, HG00464, HG00543, HG00560, HG00629, HG00443, HG00596, HG00557, HG00428, HG00653, HG00577, HG00701, HG00657, HG00475, HG00436, HG00556, HG00584, HG00533, HG00583, HG00500, HG00708, HG00692, HG00635, HG00690, HG00404, HG00531, HG00479, HG00684, HG00613, HG00525, HG00704, HG00463, HG00611, HG00476, HG00625, HG00565, HG00580, HG00473, HG00607, HG00418, HG00620, HG00707, HG00672, HG00614, HG00513, HG00578, HG00478, HG00421, HG00656, HG00698, HG00595, HG00472, HG00628, HG00581

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2676468

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	84
Observed Complex	0
Frequency	n/a