Variant Details

Variant: esv3636184

Internal ID

7022980

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr15:37975354..37976110	hg38	UCSC Ensembl
Inner	chr15:37975355..37976109	hg38	UCSC Ensembl
Outer	chr15:37975353..37976111	hg38	UCSC Ensembl
	chr15:38267555..38268311	hg19	UCSC Ensembl
Inner	chr15:38267556..38268310	hg19	UCSC Ensembl
Outer	chr15:38267554..38268312	hg19	UCSC Ensembl

Cytoband

15q14

Allele length

Assembly	Allele length
hg38	757
hg19	757

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv15220333, essv15220272, essv15220318, essv15220273, essv15220372, essv15220303, essv15220288, essv15220283, essv15220269, essv15220334, essv15220331, essv15220370, essv15220316, essv15220345, essv15220368, essv15220349, essv15220324, essv15220361, essv15220311, essv15220309, essv15220264, essv15220342, essv15220313, essv15220374, essv15220279, essv15220300, essv15220296, essv15220322, essv15220297, essv15220299, essv15220287, essv15220258, essv15220305, essv15220278, essv15220355, essv15220360, essv15220321, essv15220340, essv15220365, essv15220301, essv15220341, essv15220338, essv15220351, essv15220263, essv15220314, essv15220276, essv15220352, essv15220275, essv15220257, essv15220330, essv15220378, essv15220268, essv15220260, essv15220350, essv15220343, essv15220271, essv15220262, essv15220332, essv15220358, essv15220325, essv15220291, essv15220356, essv15220284, essv15220302, essv15220363, essv15220353, essv15220274, essv15220317, essv15220328, essv15220280, essv15220369, essv15220362, essv15220290, essv15220323, essv15220346, essv15220289, essv15220329, essv15220376, essv15220320, essv15220354, essv15220266, essv15220282, essv15220277, essv15220357, essv15220293, essv15220367, essv15220327, essv15220307, essv15220259, essv15220319, essv15220281, essv15220261, essv15220294, essv15220337, essv15220347, essv15220375, essv15220304, essv15220306, essv15220336, essv15220359, essv15220308, essv15220335, essv15220371, essv15220344, essv15220364, essv15220285, essv15220265, essv15220286, essv15220310, essv15220348, essv15220326, essv15220339, essv15220377, essv15220292, essv15220267, essv15220373, essv15220366, essv15220270, essv15220256, essv15220295, essv15220312, essv15220315, essv15220298

Samples

HG02574, NA20339, HG03559, HG02610, HG03484, NA19397, HG02583, NA18861, HG03175, NA19378, NA18507, HG02318, HG03115, HG02012, NA19350, HG03130, NA19092, HG02476, HG03190, NA18878, HG03100, NA18504, NA20332, NA19377, NA20346, HG03577, HG03172, NA19190, NA19314, HG03572, HG03464, NA19201, HG02810, NA18923, HG02620, HG02854, NA19197, HG03246, HG03105, NA19138, NA19038, HG02573, HG03045, HG02642, HG02571, HG03073, NA19025, NA19451, NA19200, NA19027, HG02819, HG02716, HG03343, HG03120, NA19908, NA19707, HG03511, NA19403, NA19152, NA19184, HG01879, NA19236, HG02144, NA18871, HG03159, HG02508, HG01880, NA19776, HG03124, HG01390, HG03301, HG03085, NA18499, NA19031, HG03571, HG03391, HG02979, HG02666, NA19160, NA19095, HG02635, NA18858, HG01990, HG01896, NA19436, NA19375, NA19308, HG02330, NA19834, NA19149, NA19147, HG02799, NA19434, HG02501, HG02308, NA19435, NA19037, HG01958, NA20351, NA19334, HG02982, HG03127, NA19324, HG02317, NA20281, HG02814, HG02558, NA19818, NA19223, HG03097, HG03049, NA19474, HG03063, HG03351, HG03162, NA19146, NA18488, NA18511, HG02643, HG03303, HG03439, NA19346, HG01507

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3636184

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	123
Observed Complex	0
Frequency	n/a