Variant Details

Variant: esv2659945

Internal ID

9926050

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:3395168..3594274	hg38	UCSC Ensembl
	chr11:3416398..3615504	hg19	UCSC Ensembl

Cytoband

11p15.4

Allele length

Assembly	Allele length
hg38	199107
hg19	199107

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5893156, essv6348746, essv6306032, essv5958119, essv6088459, essv5719548, essv6467617, essv5444906, essv6471358, essv6538949, essv5585434, essv5720902, essv5755159, essv5493037, essv6566732, essv5639017, essv5900323, essv5455536, essv5634912, essv6463556, essv6261514, essv6251156, essv5651729, essv5702558, essv6083712, essv6494139, essv5665828, essv5604023, essv5957353, essv5894975, essv6149979, essv5840108, essv6258883, essv5789770, essv5882926, essv5678448, essv5416655, essv6223606, essv6365421, essv5667779, essv6206020, essv6480571, essv6289200, essv6555574, essv5928222, essv5812988, essv5848819, essv6069151, essv5854149, essv5686953, essv5959266, essv5572003, essv5570902, essv5863481

Samples

NA19466, NA11933, NA12155, HG01140, NA19381, HG00120, NA18874, HG00325, HG00534, NA19385, NA19317, HG01440, NA19901, NA19445, NA18908, HG01124, HG01136, NA19056, NA19403, NA12342, HG00428, NA20521, HG01498, HG00250, HG00684, NA19750, NA19453, HG01497, NA20282, NA19099, NA19469, NA19440, NA19390, NA18535, NA19434, NA19072, NA12272, NA19444, NA19331, NA19428, NA19083, HG01342, HG01491, NA19468, HG00186, NA19102, NA18873, NA11843, NA19711, HG00595, HG01125, NA20322, HG01112, NA18487

Known Genes

LOC650368

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)

esv2659945

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	54
Observed Complex	0
Frequency	n/a