Variant Details

Variant: esv3596681

Internal ID

6983995

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr3:78293509..78294026	hg38	UCSC Ensembl
Inner	chr3:78293511..78294025	hg38	UCSC Ensembl
Outer	chr3:78293508..78294028	hg38	UCSC Ensembl
	chr3:78342659..78343176	hg19	UCSC Ensembl
Inner	chr3:78342661..78343175	hg19	UCSC Ensembl
Outer	chr3:78342658..78343178	hg19	UCSC Ensembl

Cytoband

3p12.3

Allele length

Assembly	Allele length
hg38	518
hg19	518

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv11049207, essv11049181, essv11049196, essv11049228, essv11049222, essv11049187, essv11049172, essv11049170, essv11049241, essv11049192, essv11049246, essv11049183, essv11049252, essv11049262, essv11049224, essv11049204, essv11049256, essv11049242, essv11049194, essv11049255, essv11049237, essv11049253, essv11049227, essv11049178, essv11049176, essv11049175, essv11049259, essv11049211, essv11049232, essv11049209, essv11049248, essv11049251, essv11049193, essv11049243, essv11049220, essv11049226, essv11049210, essv11049179, essv11049217, essv11049258, essv11049180, essv11049221, essv11049236, essv11049261, essv11049229, essv11049254, essv11049264, essv11049186, essv11049202, essv11049177, essv11049200, essv11049219, essv11049206, essv11049249, essv11049185, essv11049216, essv11049208, essv11049199, essv11049215, essv11049230, essv11049182, essv11049203, essv11049188, essv11049173, essv11049197, essv11049244, essv11049189, essv11049213, essv11049198, essv11049239, essv11049195, essv11049247, essv11049174, essv11049218, essv11049225, essv11049245, essv11049263, essv11049184, essv11049223, essv11049171, essv11049191, essv11049250, essv11049201, essv11049260, essv11049235, essv11049214, essv11049234, essv11049205, essv11049240, essv11049231, essv11049190, essv11049233, essv11049238, essv11049257, essv11049212

Samples

HG03514, NA19703, HG03052, NA19704, HG03449, NA19020, HG02476, HG03100, HG03139, HG02536, NA20356, NA19920, HG02895, HG02769, NA19107, HG03133, NA18519, HG03452, HG03499, HG02952, NA19119, NA18498, HG03224, HG03040, HG02981, HG02281, HG02315, NA18868, HG03212, HG02461, NA19372, NA19238, HG02642, NA19026, NA19901, NA20342, NA19209, NA18908, HG03114, HG03048, HG02977, NA19247, HG03054, HG03511, HG03088, HG01104, NA19152, NA19984, HG03291, HG01882, HG01879, NA19455, HG03457, HG02953, HG02307, HG01077, HG03159, HG02968, HG01880, HG03472, HG03301, HG03136, HG03476, NA18499, NA18912, HG02881, HG03451, HG02586, HG02568, HG01956, HG01990, HG02667, NA18909, NA19108, NA19147, NA20276, HG02546, HG02721, HG03458, NA19331, HG01958, HG02611, HG03433, NA19117, HG02974, HG02095, HG02970, HG02646, HG03410, HG01105, HG02051, HG03445, HG03162, NA19146, HG03198

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3596681

Frequency

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