Variant Details

Variant: esv3641592

Internal ID

7028366

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr18:3335192..3336636	hg38	UCSC Ensembl
Inner	chr18:3335193..3336636	hg38	UCSC Ensembl
Outer	chr18:3335192..3336637	hg38	UCSC Ensembl
	chr18:3335190..3336634	hg19	UCSC Ensembl
Inner	chr18:3335191..3336634	hg19	UCSC Ensembl
Outer	chr18:3335190..3336635	hg19	UCSC Ensembl

Cytoband

18p11.31

Allele length

Assembly	Allele length
hg38	1445
hg19	1445

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv15779312, essv15779282, essv15779290, essv15779309, essv15779315, essv15779294, essv15779285, essv15779281, essv15779273, essv15779284, essv15779286, essv15779298, essv15779316, essv15779307, essv15779308, essv15779293, essv15779305, essv15779275, essv15779300, essv15779278, essv15779318, essv15779301, essv15779280, essv15779302, essv15779296, essv15779317, essv15779297, essv15779311, essv15779304, essv15779299, essv15779313, essv15779291, essv15779277, essv15779314, essv15779303, essv15779274, essv15779310, essv15779287, essv15779276, essv15779292, essv15779288, essv15779295, essv15779279, essv15779306, essv15779289, essv15779283

Samples

HG01485, NA19028, NA19141, HG02944, HG03548, HG03449, NA18486, NA20294, NA19355, NA18519, HG03086, HG01167, HG02143, NA19372, HG02588, HG03225, HG02623, NA19025, HG03583, NA19027, HG02879, HG02009, HG02439, HG01989, HG02307, HG02555, HG03085, HG03476, NA19042, HG02896, HG01988, HG02675, HG03567, NA20296, HG02557, NA19712, HG03433, NA19248, HG03157, HG03049, NA19474, NA18873, HG03410, HG03401, HG02465, HG02851

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3641592

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	46
Observed Complex	0
Frequency	n/a