Variant Details

Variant: esv3635610

Internal ID

7022409

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr14:103851243..103851821	hg38	UCSC Ensembl
Inner	chr14:103851293..103851771	hg38	UCSC Ensembl
Outer	chr14:103851163..103851901	hg38	UCSC Ensembl
	chr14:104317580..104318158	hg19	UCSC Ensembl
Inner	chr14:104317630..104318108	hg19	UCSC Ensembl
Outer	chr14:104317500..104318238	hg19	UCSC Ensembl

Cytoband

14q32.33

Allele length

Assembly	Allele length
hg38	579
hg19	579

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv15114588, essv15114668, essv15114655, essv15114604, essv15114618, essv15114643, essv15114641, essv15114658, essv15114636, essv15114596, essv15114620, essv15114665, essv15114645, essv15114635, essv15114608, essv15114615, essv15114600, essv15114613, essv15114678, essv15114621, essv15114671, essv15114666, essv15114633, essv15114626, essv15114630, essv15114659, essv15114650, essv15114606, essv15114676, essv15114675, essv15114663, essv15114627, essv15114651, essv15114611, essv15114629, essv15114593, essv15114654, essv15114669, essv15114617, essv15114609, essv15114628, essv15114592, essv15114656, essv15114660, essv15114646, essv15114652, essv15114673, essv15114597, essv15114622, essv15114591, essv15114598, essv15114681, essv15114664, essv15114614, essv15114653, essv15114679, essv15114583, essv15114619, essv15114616, essv15114639, essv15114602, essv15114594, essv15114672, essv15114632, essv15114662, essv15114612, essv15114601, essv15114667, essv15114640, essv15114605, essv15114649, essv15114624, essv15114595, essv15114625, essv15114607, essv15114682, essv15114647, essv15114610, essv15114680, essv15114631, essv15114634, essv15114599, essv15114648, essv15114657, essv15114589, essv15114585, essv15114637, essv15114581, essv15114674, essv15114638, essv15114584, essv15114661, essv15114677, essv15114603, essv15114580, essv15114582, essv15114644, essv15114587, essv15114623, essv15114642, essv15114586, essv15114590, essv15114670

Samples

HG02386, HG01402, HG01965, HG03378, HG03228, HG03738, HG02337, HG02727, NA19350, NA18878, HG01944, NA18962, HG00663, HG03572, HG02811, NA19723, HG02840, NA20911, HG03673, NA18960, HG03342, NA19088, NA18571, HG02054, HG00451, NA19038, NA19041, HG02512, NA18977, NA19385, NA18986, HG02502, NA21114, NA18954, HG03270, HG03169, HG01699, HG03908, HG03054, HG01867, NA19082, HG00982, HG03061, HG03511, HG04146, HG02090, NA19086, HG01864, NA18644, NA18939, HG02953, NA18566, HG03742, NA19118, HG02577, HG00350, NA20856, HG01921, HG04017, HG02283, NA19740, HG01403, HG02332, HG01589, NA18646, HG02484, NA18608, HG03848, HG03240, NA19149, NA19735, NA19072, HG03949, HG01915, HG03689, NA20902, NA18643, NA19741, HG02139, HG02137, NA18615, HG04141, NA19323, HG01395, HG04015, NA21090, HG03977, HG03733, HG02699, HG03279, HG03063, NA21093, HG03916, NA20786, HG02774, HG01431, HG02028, NA19312, NA19463, HG03198, HG01923, HG00978, HG03196

Known Genes

LINC00637

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3635610

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	103
Observed Complex	0
Frequency	n/a