Variant Details

Variant: esv3635415

Internal ID

7022214

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr14:96115202..96115542	hg38	UCSC Ensembl
Inner	chr14:96115202..96115542	hg38	UCSC Ensembl
Outer	chr14:96114752..96115815	hg38	UCSC Ensembl
	chr14:96581539..96581879	hg19	UCSC Ensembl
Inner	chr14:96581539..96581879	hg19	UCSC Ensembl
Outer	chr14:96581089..96582152	hg19	UCSC Ensembl

Cytoband

14q32.2

Allele length

Assembly	Allele length
hg38	341
hg19	341

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv15103442, essv15103441, essv15103462, essv15103458, essv15103456, essv15103479, essv15103480, essv15103475, essv15103449, essv15103463, essv15103473, essv15103437, essv15103454, essv15103435, essv15103478, essv15103466, essv15103447, essv15103472, essv15103481, essv15103445, essv15103455, essv15103446, essv15103459, essv15103474, essv15103452, essv15103439, essv15103461, essv15103471, essv15103464, essv15103469, essv15103476, essv15103444, essv15103451, essv15103468, essv15103443, essv15103457, essv15103467, essv15103453, essv15103448, essv15103438, essv15103477, essv15103460, essv15103465, essv15103470, essv15103436, essv15103440, essv15103450

Samples

NA18502, NA19222, HG01402, HG03484, HG02628, HG02481, NA19399, HG02337, NA18917, NA18877, HG03558, NA19777, NA19920, HG03478, NA19107, NA19374, HG00641, HG03464, HG03499, HG02325, NA19041, NA19372, NA19026, HG03055, HG02715, HG03363, NA19707, HG02307, HG02508, HG02014, HG02497, HG02470, HG03391, HG01403, HG01988, NA19625, HG01075, HG02613, NA19256, HG02010, HG02611, HG02317, NA19468, HG02462, NA18876, HG03470, NA19676

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3635415

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	47
Observed Complex	0
Frequency	n/a