Variant Details

Variant: esv3633721

Internal ID

7020528

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr14:21558148..21568151	hg38	UCSC Ensembl
Inner	chr14:21558298..21568001	hg38	UCSC Ensembl
Outer	chr14:21557998..21568301	hg38	UCSC Ensembl
	chr14:22026279..22036282	hg19	UCSC Ensembl
Inner	chr14:22026429..22036132	hg19	UCSC Ensembl
Outer	chr14:22026129..22036432	hg19	UCSC Ensembl

Cytoband

14q11.2

Allele length

Assembly	Allele length
hg38	10004
hg19	10004

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv14930220, essv14930183, essv14930196, essv14930141, essv14930235, essv14930150, essv14930230, essv14930153, essv14930197, essv14930167, essv14930203, essv14930171, essv14930227, essv14930182, essv14930211, essv14930186, essv14930154, essv14930147, essv14930207, essv14930193, essv14930212, essv14930215, essv14930149, essv14930169, essv14930206, essv14930159, essv14930242, essv14930241, essv14930237, essv14930175, essv14930244, essv14930228, essv14930190, essv14930195, essv14930219, essv14930170, essv14930204, essv14930187, essv14930162, essv14930210, essv14930191, essv14930239, essv14930199, essv14930140, essv14930163, essv14930232, essv14930205, essv14930240, essv14930222, essv14930177, essv14930173, essv14930201, essv14930188, essv14930146, essv14930218, essv14930157, essv14930152, essv14930172, essv14930236, essv14930184, essv14930214, essv14930216, essv14930213, essv14930165, essv14930168, essv14930209, essv14930223, essv14930238, essv14930166, essv14930143, essv14930148, essv14930194, essv14930234, essv14930185, essv14930221, essv14930174, essv14930189, essv14930160, essv14930226, essv14930142, essv14930224, essv14930179, essv14930151, essv14930176, essv14930200, essv14930155, essv14930180, essv14930145, essv14930144, essv14930233, essv14930181, essv14930158, essv14930229, essv14930217, essv14930243, essv14930202, essv14930156, essv14930231, essv14930225, essv14930208, essv14930198, essv14930178, essv14930164, essv14930161, essv14930192

Samples

HG01985, HG02574, HG03559, NA19397, HG02583, NA18861, HG02973, HG02702, HG02318, HG02419, HG02798, NA19020, NA20294, HG01971, HG03518, HG03297, HG03139, HG02895, HG03478, HG03572, HG02621, NA19319, NA19448, HG02325, NA18923, NA19198, HG01710, HG02860, HG02854, HG02111, NA19130, HG02489, NA19038, HG02562, HG03520, HG02561, HG02573, NA20340, NA19385, HG03352, NA19036, HG03225, NA19456, NA19025, HG03270, HG02879, HG02716, HG02009, HG02943, HG02442, NA19247, NA19210, HG03132, HG03363, HG03291, HG03428, HG02953, HG01989, HG02508, HG03027, NA18907, NA18499, HG02884, HG03451, NA19338, NA18523, NA19318, NA19160, HG02896, NA18858, HG03109, HG01956, HG01896, NA19035, HG02255, NA19149, NA19019, HG01551, NA19435, HG03458, NA19331, HG01933, HG02771, NA20357, NA19376, NA19328, HG03565, HG03112, HG01912, HG02053, NA19474, HG03063, NA19102, NA18876, NA19711, NA19213, HG03077, HG03538, HG02763, NA19146, NA19312, HG02629, NA19214, NA19153, HG02760

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3633721

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	105
Observed Complex	0
Frequency	n/a