Variant Details

Variant: esv3621011

Internal ID

7007881

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr9:88793432..88794303	hg38	UCSC Ensembl
Inner	chr9:88793457..88794279	hg38	UCSC Ensembl
Outer	chr9:88793408..88794328	hg38	UCSC Ensembl
	chr9:91408347..91409218	hg19	UCSC Ensembl
Inner	chr9:91408372..91409194	hg19	UCSC Ensembl
Outer	chr9:91408323..91409243	hg19	UCSC Ensembl

Cytoband

9q22.1

Allele length

Assembly	Allele length
hg38	872
hg19	872

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv13549402, essv13549439, essv13549386, essv13549416, essv13549448, essv13549449, essv13549437, essv13549421, essv13549395, essv13549441, essv13549457, essv13549414, essv13549454, essv13549405, essv13549417, essv13549447, essv13549397, essv13549431, essv13549442, essv13549418, essv13549432, essv13549472, essv13549403, essv13549425, essv13549420, essv13549473, essv13549415, essv13549433, essv13549400, essv13549410, essv13549467, essv13549412, essv13549463, essv13549452, essv13549393, essv13549474, essv13549444, essv13549396, essv13549461, essv13549406, essv13549470, essv13549404, essv13549399, essv13549443, essv13549411, essv13549464, essv13549428, essv13549462, essv13549384, essv13549471, essv13549409, essv13549401, essv13549476, essv13549466, essv13549382, essv13549436, essv13549465, essv13549408, essv13549394, essv13549450, essv13549426, essv13549389, essv13549423, essv13549456, essv13549453, essv13549383, essv13549475, essv13549427, essv13549391, essv13549460, essv13549407, essv13549435, essv13549429, essv13549413, essv13549446, essv13549430, essv13549469, essv13549424, essv13549422, essv13549458, essv13549455, essv13549445, essv13549398, essv13549392, essv13549388, essv13549468, essv13549440, essv13549434, essv13549419, essv13549451, essv13549459, essv13549438, essv13549387, essv13549385, essv13549390

Samples

HG00114, HG01098, NA12842, HG00143, NA19794, NA12286, HG01443, HG02298, HG01389, HG01066, HG04094, HG01686, HG00150, NA20517, NA20507, HG01632, HG01924, HG00138, HG01506, HG01350, NA20774, HG03765, HG00330, HG01492, NA07048, NA07347, HG03911, HG01668, NA20539, HG01069, HG01080, HG00148, NA20819, HG01072, HG01767, HG01405, HG01176, HG01525, HG00182, HG00118, NA12828, NA20787, HG04225, HG00145, HG01669, HG01088, HG00344, HG01345, HG00239, HG01092, NA20525, HG01102, HG00250, NA20901, HG03713, HG00331, HG01613, HG01383, HG03953, HG03854, HG03745, HG01334, HG01403, NA20828, HG02219, NA20542, HG01107, HG01204, HG01530, NA20765, NA20296, NA20821, HG00258, HG03848, NA12716, HG04216, HG03790, HG01190, HG01980, HG01678, HG02682, HG00734, HG01357, HG01375, HG01205, NA20797, HG01432, HG01302, HG01254, HG01756, HG03890, HG01672, NA20827, HG01097, NA20511

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3621011

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	95
Observed Complex	0
Frequency	n/a