Variant Details

Variant: esv3627830

Internal ID

7014655

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:116797581..116802941	hg38	UCSC Ensembl
Inner	chr11:116797902..116802881	hg38	UCSC Ensembl
Outer	chr11:116797417..116803105	hg38	UCSC Ensembl
	chr11:116668297..116673657	hg19	UCSC Ensembl
Inner	chr11:116668618..116673597	hg19	UCSC Ensembl
Outer	chr11:116668133..116673821	hg19	UCSC Ensembl

Cytoband

11q23.3

Allele length

Assembly	Allele length
hg38	5361
hg19	5361

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv14291902, essv14291929, essv14291884, essv14291863, essv14291852, essv14291911, essv14291862, essv14291915, essv14291836, essv14291904, essv14291905, essv14291864, essv14291922, essv14291908, essv14291913, essv14291919, essv14291838, essv14291883, essv14291854, essv14291846, essv14291879, essv14291924, essv14291840, essv14291903, essv14291868, essv14291870, essv14291878, essv14291890, essv14291892, essv14291866, essv14291895, essv14291894, essv14291844, essv14291845, essv14291910, essv14291921, essv14291927, essv14291835, essv14291932, essv14291901, essv14291831, essv14291885, essv14291931, essv14291881, essv14291887, essv14291853, essv14291841, essv14291928, essv14291847, essv14291896, essv14291859, essv14291855, essv14291843, essv14291829, essv14291851, essv14291867, essv14291925, essv14291834, essv14291914, essv14291869, essv14291930, essv14291926, essv14291832, essv14291871, essv14291923, essv14291842, essv14291833, essv14291873, essv14291874, essv14291906, essv14291899, essv14291858, essv14291909, essv14291876, essv14291857, essv14291830, essv14291917, essv14291889, essv14291886, essv14291907, essv14291893, essv14291856, essv14291837, essv14291912, essv14291888, essv14291839, essv14291850, essv14291875, essv14291882, essv14291861, essv14291880, essv14291918, essv14291933, essv14291865, essv14291860, essv14291898, essv14291877, essv14291849, essv14291916, essv14291920, essv14291872, essv14291897, essv14291900, essv14291891, essv14291848

Samples

HG03096, HG01485, HG02339, NA19141, HG01412, HG02610, HG02628, HG03378, HG02481, NA18881, HG03241, HG02852, NA19795, HG02870, NA18878, NA18504, HG03126, HG00737, HG03193, HG02536, HG01953, HG02810, NA18489, NA19448, HG03091, NA19198, HG03370, HG02645, HG02922, HG02111, HG02981, HG02315, HG03268, NA18868, HG03195, HG02642, HG01308, NA19471, HG02502, NA19189, NA19239, NA19209, NA18908, NA19210, HG03363, HG02334, NA19175, NA19462, HG03547, HG02511, NA18516, HG03428, HG03159, HG03081, HG01880, HG01323, HG01889, HG02757, HG03294, HG02555, HG01161, NA19449, HG03476, NA19113, NA18912, NA18853, HG02979, HG02635, HG02594, HG02568, HG01896, HG02772, NA20296, HG02667, HG03240, NA19834, HG03461, NA19149, HG03539, HG02308, HG02983, HG02837, NA19144, NA18865, HG03304, HG02839, HG02558, HG02971, NA19248, NA19351, HG02053, HG02462, HG02676, NA18873, NA19096, NA19213, NA19121, NA19030, HG03162, NA19146, NA19463, HG03118, HG02006, HG00553, HG02760

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3627830

Frequency

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