Variant Details

Variant: esv2656698

Internal ID

9922803

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr6:2567941..2571694	hg38	UCSC Ensembl
	chr6:2568175..2571928	hg19	UCSC Ensembl

Cytoband

6p25.2

Allele length

Assembly	Allele length
hg38	3754
hg19	3754

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv1069e199

Supporting Variants

essv6094940, essv5973910, essv6528143, essv5396687, essv6302065, essv6196177, essv6167697, essv5632821, essv5989999, essv5613380, essv6547465, essv6297975, essv5900815, essv5897999, essv5876370, essv6370474, essv6111602, essv5701197, essv5566883, essv6058804, essv6484358, essv6351659, essv6194937, essv6134616, essv5616418, essv6089044, essv5518076, essv5761658, essv6085247, essv6148632, essv5897248, essv5602956, essv6410049, essv5923596, essv5928875, essv6162756, essv6151040, essv6487997, essv5602801, essv6187003, essv6301982, essv6009404, essv6040940, essv5415277, essv5672534, essv5914230, essv6019314, essv5767137, essv6552876, essv6508825, essv5962760, essv6453789, essv6245209, essv6168640, essv6114257, essv6450701, essv6516049, essv5738182, essv6440659, essv5452021, essv5440040, essv6347973, essv6142999, essv5814150, essv5673579, essv6015768, essv6040308, essv5937301, essv5693011, essv6099255, essv6036776, essv6515204, essv5720975, essv6433588, essv5952691, essv5896081, essv6422089, essv5497310, essv5921637, essv5529963, essv6230226, essv5444096, essv5849280, essv6448034, essv5462723, essv6248963, essv6050788, essv5661745, essv6570857, essv6035659, essv6051039, essv5994914, essv5955227, essv6184885, essv5927978, essv5593049, essv5821361, essv6396322, essv5959355, essv5896025, essv5618343, essv5843619, essv5939541, essv6361789, essv5997662, essv5969695

Samples

HG00096, NA19701, NA11830, NA19700, NA19397, NA18924, HG01462, NA19909, NA20766, NA20508, NA19204, NA18508, NA19399, NA19332, HG01389, HG00318, NA19359, NA19819, NA19393, NA18504, NA20332, NA20517, NA12400, HG01051, NA18510, HG01140, NA20814, NA07346, NA19374, NA19396, NA19381, NA19379, NA18519, HG01366, HG00122, NA18489, NA19448, NA19131, NA18916, NA11918, NA07347, NA19313, NA19138, NA18498, NA19904, NA19384, NA12761, NA19383, HG00236, HG01072, NA19372, NA19385, HG00118, NA19189, NA19209, NA19789, NA19200, HG00739, HG01353, HG00137, HG00188, NA19707, NA19403, HG00245, NA18933, NA19391, NA19327, NA19236, NA20344, NA19654, NA18499, HG01383, NA19453, NA18912, NA19761, HG00146, NA19225, NA18523, NA19318, NA20799, NA20801, NA18909, NA19712, NA19435, NA19444, NA19380, NA19835, NA19334, NA19439, NA19428, NA19324, NA19311, HG01137, HG00116, HG01108, NA07037, HG00256, NA19376, NA19248, NA20582, NA19474, HG01055, NA18873, NA19116, NA18511, HG00553

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

High quality site

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2656698

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	106
Observed Complex	0
Frequency	n/a