Variant Details

Variant: esv3597318

Internal ID

6984546

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr3:107983483..107986209	hg38	UCSC Ensembl
Inner	chr3:107983983..107985709	hg38	UCSC Ensembl
Outer	chr3:107982483..107987209	hg38	UCSC Ensembl
	chr3:107702330..107705056	hg19	UCSC Ensembl
Inner	chr3:107702830..107704556	hg19	UCSC Ensembl
Outer	chr3:107701330..107706056	hg19	UCSC Ensembl

Cytoband

3q13.12

Allele length

Assembly	Allele length
hg38	2727
hg19	2727

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv11096632, essv11096630, essv11096624, essv11096631, essv11096615, essv11096633, essv11096616, essv11096613, essv11096596, essv11096638, essv11096598, essv11096636, essv11096603, essv11096608, essv11096635, essv11096609, essv11096610, essv11096600, essv11096614, essv11096606, essv11096602, essv11096634, essv11096619, essv11096618, essv11096625, essv11096604, essv11096637, essv11096607, essv11096623, essv11096627, essv11096599, essv11096597, essv11096601, essv11096628, essv11096605, essv11096612, essv11096593, essv11096621, essv11096592, essv11096629, essv11096620, essv11096595, essv11096626, essv11096611, essv11096622, essv11096617, essv11096594

Samples

HG01441, HG01462, HG01961, HG02275, NA19777, HG00737, HG01947, HG02285, HG01341, HG02105, HG01968, HG02299, HG01982, HG01372, HG01893, HG01134, HG01495, HG01440, NA19725, HG01048, HG01942, HG02265, HG01187, HG01149, NA19776, HG01092, NA19654, HG01383, NA19740, NA19761, NA19682, HG02286, HG01403, HG01444, NA19652, HG02089, NA19732, HG01551, HG01253, HG02304, HG01357, NA19741, HG01577, HG02147, NA19780, NA19758, HG01125

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3597318

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	47
Observed Complex	0
Frequency	n/a