Variant Details

Variant: esv3611230

Internal ID

6998141

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr6:150322292..150326710	hg38	UCSC Ensembl
Inner	chr6:150322293..150326710	hg38	UCSC Ensembl
Outer	chr6:150322292..150326711	hg38	UCSC Ensembl
	chr6:150643428..150647846	hg19	UCSC Ensembl
Inner	chr6:150643429..150647846	hg19	UCSC Ensembl
Outer	chr6:150643428..150647847	hg19	UCSC Ensembl

Cytoband

6q25.1

Allele length

Assembly	Allele length
hg38	4419
hg19	4419

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv12581287, essv12581271, essv12581214, essv12581289, essv12581281, essv12581288, essv12581224, essv12581217, essv12581215, essv12581250, essv12581254, essv12581230, essv12581222, essv12581280, essv12581261, essv12581251, essv12581272, essv12581208, essv12581274, essv12581262, essv12581286, essv12581299, essv12581221, essv12581219, essv12581228, essv12581253, essv12581233, essv12581223, essv12581239, essv12581295, essv12581236, essv12581229, essv12581301, essv12581248, essv12581279, essv12581285, essv12581268, essv12581256, essv12581283, essv12581209, essv12581227, essv12581292, essv12581263, essv12581242, essv12581278, essv12581258, essv12581276, essv12581243, essv12581293, essv12581216, essv12581304, essv12581252, essv12581211, essv12581303, essv12581264, essv12581226, essv12581269, essv12581270, essv12581212, essv12581235, essv12581249, essv12581231, essv12581300, essv12581265, essv12581275, essv12581245, essv12581296, essv12581302, essv12581291, essv12581266, essv12581225, essv12581290, essv12581237, essv12581260, essv12581240, essv12581213, essv12581255, essv12581206, essv12581205, essv12581232, essv12581257, essv12581241, essv12581218, essv12581220, essv12581297, essv12581259, essv12581246, essv12581282, essv12581244, essv12581267, essv12581238, essv12581298, essv12581277, essv12581273, essv12581234, essv12581210, essv12581207, essv12581284, essv12581247, essv12581294

Samples

NA18502, HG02339, HG02944, HG02610, HG01885, NA19399, HG03241, HG03449, HG02852, HG02798, HG03115, NA20321, HG03280, HG03515, HG02895, HG03074, NA19374, HG03086, HG02621, NA19319, HG03099, NA18489, HG02756, HG02620, NA19131, NA18916, NA19197, NA19782, NA19904, NA19384, NA20291, HG02281, NA19923, HG02703, HG02315, HG01757, NA19159, NA20412, HG02946, NA19239, HG03055, HG03394, HG02882, HG03048, HG01124, HG03054, HG03061, HG02678, HG01323, HG01149, HG01889, HG02429, NA19449, NA18499, HG03078, HG02283, HG01130, NA18853, HG03024, NA19099, HG01286, NA19318, HG02332, HG02896, HG02594, NA18858, HG01956, HG02675, HG01896, HG02722, HG02455, NA19206, HG02667, HG02557, NA19712, HG02546, HG02611, NA19835, HG02839, HG02464, HG03565, HG02970, HG03097, HG03066, NA19468, HG03060, HG02462, NA19185, NA19102, HG03077, HG02052, HG01883, NA19030, HG02763, HG03072, HG02851, NA18522, HG03129, NA19153, HG01747

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3611230

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	100
Observed Complex	0
Frequency	n/a