Variant Details

Variant: esv3647673

Internal ID

7034413

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr22:35737423..35738203	hg38	UCSC Ensembl
Inner	chr22:35737425..35738202	hg38	UCSC Ensembl
Outer	chr22:35737422..35738205	hg38	UCSC Ensembl
	chr22:36133470..36134250	hg19	UCSC Ensembl
Inner	chr22:36133472..36134249	hg19	UCSC Ensembl
Outer	chr22:36133469..36134252	hg19	UCSC Ensembl

Cytoband

22q12.3

Allele length

Assembly	Allele length
hg38	781
hg19	781

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv16413456, essv16413492, essv16413448, essv16413442, essv16413468, essv16413512, essv16413451, essv16413434, essv16413444, essv16413514, essv16413465, essv16413490, essv16413488, essv16413494, essv16413466, essv16413509, essv16413489, essv16413513, essv16413446, essv16413452, essv16413510, essv16413484, essv16413476, essv16413475, essv16413478, essv16413496, essv16413453, essv16413462, essv16413482, essv16413485, essv16413458, essv16413473, essv16413433, essv16413477, essv16413502, essv16413454, essv16413481, essv16413508, essv16413498, essv16413450, essv16413459, essv16413483, essv16413445, essv16413432, essv16413507, essv16413495, essv16413463, essv16413472, essv16413437, essv16413440, essv16413511, essv16413503, essv16413504, essv16413491, essv16413497, essv16413516, essv16413515, essv16413501, essv16413435, essv16413455, essv16413479, essv16413493, essv16413460, essv16413470, essv16413500, essv16413438, essv16413499, essv16413487, essv16413436, essv16413443, essv16413457, essv16413469, essv16413467, essv16413474, essv16413464, essv16413439, essv16413480, essv16413461, essv16413486, essv16413441, essv16413506, essv16413449, essv16413471, essv16413505, essv16413447

Samples

NA19648, HG01098, NA21089, NA21100, NA12843, HG01280, NA12751, HG03941, HG02600, HG01971, HG02215, NA19669, NA21128, NA12750, NA12399, HG00641, HG01682, NA20589, HG01064, NA11992, HG03868, NA20539, NA20819, NA06984, HG02224, HG03777, HG04020, HG02502, HG00118, NA20533, HG03585, NA21105, HG01524, NA11831, HG00137, NA20854, HG01171, NA20858, HG02233, HG01200, HG01670, HG00328, HG01790, NA20862, HG02102, NA20770, HG01049, NA21116, HG01094, HG04017, HG01130, HG01497, HG04063, HG03854, HG00246, HG00258, HG00155, HG03790, NA21144, HG00742, HG03949, NA20527, HG01623, NA12763, HG01785, NA06994, HG01577, HG00259, NA21088, NA12749, HG02235, HG01302, HG00131, HG02681, HG02051, HG00105, HG01617, NA21104, HG01509, HG01695, NA12776, NA20509, NA19676, HG01516, HG01608

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3647673

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	85
Observed Complex	0
Frequency	n/a