Variant Details

Variant: esv3641626

Internal ID

7028400

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr18:4506390..4511199	hg38	UCSC Ensembl
Inner	chr18:4506890..4510699	hg38	UCSC Ensembl
Outer	chr18:4505390..4512199	hg38	UCSC Ensembl
	chr18:4506390..4511199	hg19	UCSC Ensembl
Inner	chr18:4506890..4510699	hg19	UCSC Ensembl
Outer	chr18:4505390..4512199	hg19	UCSC Ensembl

Cytoband

18p11.31

Allele length

Assembly	Allele length
hg38	4810
hg19	4810

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv15781431, essv15781449, essv15781434, essv15781419, essv15781455, essv15781460, essv15781427, essv15781438, essv15781445, essv15781420, essv15781442, essv15781457, essv15781447, essv15781426, essv15781456, essv15781437, essv15781443, essv15781439, essv15781421, essv15781448, essv15781446, essv15781423, essv15781422, essv15781432, essv15781428, essv15781424, essv15781453, essv15781430, essv15781435, essv15781418, essv15781436, essv15781425, essv15781440, essv15781454, essv15781444, essv15781429, essv15781458, essv15781451, essv15781461, essv15781433, essv15781441, essv15781463, essv15781450, essv15781452, essv15781462, essv15781459

Samples

HG03514, NA19701, HG03484, NA18508, NA19332, HG02433, HG03241, NA18486, HG03139, HG03478, HG01924, HG03385, NA19307, HG02325, HG02816, HG01110, HG02561, NA19036, NA19451, NA19027, HG01164, HG01187, HG01171, HG03061, HG01142, NA18871, HG03382, HG03136, NA19042, HG03397, NA18856, HG02309, HG02283, NA18858, HG01107, NA19149, HG02923, HG02558, NA19117, HG02971, NA19248, NA19900, NA19121, NA19146, HG02851, HG01886

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3641626

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	46
Observed Complex	0
Frequency	n/a