Variant Details

Variant: esv3625488

Internal ID

7012322

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:18076363..18078587	hg38	UCSC Ensembl
Inner	chr11:18076364..18078587	hg38	UCSC Ensembl
Outer	chr11:18076363..18078588	hg38	UCSC Ensembl
	chr11:18097910..18100134	hg19	UCSC Ensembl
Inner	chr11:18097911..18100134	hg19	UCSC Ensembl
Outer	chr11:18097910..18100135	hg19	UCSC Ensembl

Cytoband

11p15.1

Allele length

Assembly	Allele length
hg38	2225
hg19	2225

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv14040270, essv14040288, essv14040284, essv14040239, essv14040193, essv14040230, essv14040222, essv14040256, essv14040232, essv14040200, essv14040195, essv14040296, essv14040199, essv14040237, essv14040210, essv14040255, essv14040263, essv14040246, essv14040211, essv14040278, essv14040245, essv14040259, essv14040294, essv14040281, essv14040220, essv14040242, essv14040231, essv14040280, essv14040209, essv14040215, essv14040214, essv14040264, essv14040251, essv14040206, essv14040286, essv14040250, essv14040257, essv14040196, essv14040302, essv14040291, essv14040218, essv14040213, essv14040227, essv14040228, essv14040224, essv14040249, essv14040240, essv14040192, essv14040201, essv14040276, essv14040254, essv14040203, essv14040247, essv14040279, essv14040223, essv14040208, essv14040303, essv14040260, essv14040283, essv14040267, essv14040225, essv14040282, essv14040272, essv14040258, essv14040234, essv14040233, essv14040212, essv14040289, essv14040287, essv14040273, essv14040244, essv14040300, essv14040190, essv14040216, essv14040262, essv14040221, essv14040202, essv14040269, essv14040295, essv14040277, essv14040285, essv14040248, essv14040266, essv14040219, essv14040298, essv14040293, essv14040238, essv14040236, essv14040301, essv14040235, essv14040252, essv14040265, essv14040243, essv14040197, essv14040204, essv14040253, essv14040226, essv14040194, essv14040292, essv14040207, essv14040275, essv14040290, essv14040261, essv14040191, essv14040271, essv14040268, essv14040297, essv14040205, essv14040198, essv14040229, essv14040274, essv14040241, essv14040299, essv14040217

Samples

HG01060, HG00235, HG01356, HG01773, HG01079, HG00100, HG02262, HG02727, NA20813, HG01531, HG01456, HG00150, NA12399, HG01140, NA12813, NA20814, HG00356, HG00272, HG03640, HG01488, HG00736, HG03663, NA20822, NA11918, NA21108, NA19904, NA19922, HG00139, NA12282, NA19651, HG01067, NA06984, HG01628, HG00236, HG00262, HG03947, HG01673, HG01405, HG01176, HG00182, NA19725, HG01198, NA20764, HG01121, NA12828, HG01275, NA20757, NA20818, HG01353, HG00313, HG00188, HG00176, HG00282, HG02236, HG01790, HG01789, HG02108, NA19663, HG01768, HG04035, HG01119, HG04180, HG01777, HG00324, HG01512, HG01762, HG00373, NA21141, HG00110, NA11840, HG04173, HG01182, HG01497, HG01705, HG01334, HG00099, HG01697, HG01625, HG03934, NA19729, NA11881, HG00265, HG00357, HG00136, NA20870, HG01272, NA20790, NA20778, HG00116, HG01489, NA06986, HG01086, NA20906, HG01765, HG01770, HG01491, HG00381, HG02238, NA12749, NA19716, HG00174, HG00123, HG00186, HG00234, NA19711, HG01105, HG01479, HG00372, HG01617, NA12154, HG01191, HG00180, NA12776, HG01608

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3625488

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	114
Observed Complex	0
Frequency	n/a