Variant Details

Variant: esv3627230

Internal ID

7014060

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:90971570..90977194	hg38	UCSC Ensembl
Inner	chr11:90971570..90977194	hg38	UCSC Ensembl
Outer	chr11:90971070..90977694	hg38	UCSC Ensembl
	chr11:90704738..90710362	hg19	UCSC Ensembl
Inner	chr11:90704738..90710362	hg19	UCSC Ensembl
Outer	chr11:90704238..90710862	hg19	UCSC Ensembl

Cytoband

11q14.3

Allele length

Assembly	Allele length
hg38	5625
hg19	5625

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv14232825, essv14232895, essv14232868, essv14232815, essv14232890, essv14232816, essv14232902, essv14232827, essv14232809, essv14232859, essv14232888, essv14232857, essv14232862, essv14232828, essv14232898, essv14232872, essv14232871, essv14232806, essv14232814, essv14232904, essv14232843, essv14232870, essv14232863, essv14232894, essv14232805, essv14232884, essv14232837, essv14232903, essv14232849, essv14232833, essv14232852, essv14232866, essv14232817, essv14232885, essv14232867, essv14232856, essv14232846, essv14232822, essv14232897, essv14232842, essv14232877, essv14232889, essv14232840, essv14232874, essv14232860, essv14232808, essv14232839, essv14232812, essv14232841, essv14232829, essv14232850, essv14232836, essv14232835, essv14232834, essv14232820, essv14232855, essv14232896, essv14232838, essv14232869, essv14232821, essv14232882, essv14232876, essv14232893, essv14232881, essv14232880, essv14232819, essv14232813, essv14232892, essv14232807, essv14232810, essv14232853, essv14232831, essv14232824, essv14232875, essv14232900, essv14232865, essv14232887, essv14232848, essv14232826, essv14232823, essv14232830, essv14232879, essv14232886, essv14232861, essv14232845, essv14232832, essv14232858, essv14232811, essv14232901, essv14232883, essv14232854, essv14232891, essv14232818, essv14232878, essv14232873, essv14232864, essv14232847, essv14232851, essv14232899, essv14232844

Samples

HG03559, HG01402, NA18924, HG03111, NA18881, HG03241, HG03449, HG02804, HG03521, HG03298, HG03280, NA20298, HG03455, HG03100, NA19377, HG03577, NA18870, NA18510, HG02769, HG03199, NA19448, HG02952, NA19119, HG02645, HG02922, HG02111, HG03209, HG03460, HG03189, NA18868, HG02885, NA19159, HG02946, HG02427, HG01058, NA18908, HG02882, HG02715, NA18934, HG03088, NA19175, HG02582, HG03547, NA19184, HG01882, HG02108, HG02322, NA18915, HG01989, HG01119, HG02508, NA19776, HG02757, HG03136, HG03202, NA18499, NA18856, NA18912, HG02309, HG02283, NA19740, NA18853, HG03024, HG02585, NA19160, HG02586, HG02484, HG03567, HG02772, HG02255, NA19309, HG02557, NA19108, NA19147, HG03437, HG02799, HG01958, HG02837, HG03259, HG02839, HG03473, HG02464, NA19117, HG03565, NA20348, HG02971, NA19438, NA19472, HG02938, NA19474, HG02107, NA19093, HG03258, NA19102, NA19900, HG02051, NA18984, HG02861, HG01464, HG02808

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3627230

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	100
Observed Complex	0
Frequency	n/a