Variant Details

Variant: esv3622611

Internal ID

7009469

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr10:23412217..23419420	hg38	UCSC Ensembl
Inner	chr10:23412218..23419420	hg38	UCSC Ensembl
Outer	chr10:23412217..23419421	hg38	UCSC Ensembl
	chr10:23701146..23708349	hg19	UCSC Ensembl
Inner	chr10:23701147..23708349	hg19	UCSC Ensembl
Outer	chr10:23701146..23708350	hg19	UCSC Ensembl

Cytoband

10p12.2

Allele length

Assembly	Allele length
hg38	7204
hg19	7204

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv13716132, essv13716118, essv13716133, essv13716152, essv13716126, essv13716155, essv13716131, essv13716115, essv13716127, essv13716161, essv13716157, essv13716137, essv13716162, essv13716145, essv13716143, essv13716141, essv13716153, essv13716148, essv13716154, essv13716138, essv13716134, essv13716117, essv13716158, essv13716125, essv13716146, essv13716149, essv13716119, essv13716124, essv13716129, essv13716160, essv13716139, essv13716150, essv13716135, essv13716156, essv13716142, essv13716159, essv13716151, essv13716122, essv13716121, essv13716120, essv13716144, essv13716123, essv13716140, essv13716136, essv13716147, essv13716116, essv13716130, essv13716128

Samples

NA19222, NA19397, NA18861, HG02419, NA19393, NA19377, HG03297, NA18870, HG02769, NA19446, HG03499, HG03342, NA19904, HG03079, NA19383, HG01308, NA19456, HG02882, HG02715, HG03369, HG02879, NA19152, HG02449, NA19913, HG02144, HG02953, HG02887, HG01989, HG03027, HG02470, HG01889, HG02429, NA19320, NA19452, HG02667, HG03461, HG02308, HG01551, NA19435, NA19310, NA19467, HG03419, HG02558, HG03103, HG02771, NA19117, HG01912, NA19096

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3622611

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	48
Observed Complex	0
Frequency	n/a