Variant Details

Variant: esv3587695

Internal ID

6975117

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr1:159150272..159155774	hg38	UCSC Ensembl
Inner	chr1:159150272..159155774	hg38	UCSC Ensembl
Outer	chr1:159149802..159156128	hg38	UCSC Ensembl
	chr1:159120062..159125564	hg19	UCSC Ensembl
Inner	chr1:159120062..159125564	hg19	UCSC Ensembl
Outer	chr1:159119592..159125918	hg19	UCSC Ensembl

Cytoband

1q23.2

Allele length

Assembly	Allele length
hg38	5503
hg19	5503

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv10163938, essv10163876, essv10163916, essv10163905, essv10163946, essv10163944, essv10163855, essv10163879, essv10163864, essv10163931, essv10163929, essv10163858, essv10163867, essv10163884, essv10163899, essv10163898, essv10163893, essv10163927, essv10163871, essv10163921, essv10163928, essv10163923, essv10163937, essv10163897, essv10163863, essv10163869, essv10163915, essv10163902, essv10163870, essv10163906, essv10163872, essv10163857, essv10163934, essv10163890, essv10163894, essv10163875, essv10163900, essv10163914, essv10163942, essv10163856, essv10163901, essv10163885, essv10163911, essv10163920, essv10163882, essv10163868, essv10163909, essv10163878, essv10163943, essv10163919, essv10163883, essv10163908, essv10163907, essv10163866, essv10163865, essv10163861, essv10163918, essv10163862, essv10163854, essv10163904, essv10163891, essv10163888, essv10163936, essv10163886, essv10163860, essv10163940, essv10163880, essv10163873, essv10163889, essv10163896, essv10163892, essv10163932, essv10163930, essv10163939, essv10163924, essv10163947, essv10163925, essv10163877, essv10163912, essv10163910, essv10163933, essv10163935, essv10163913, essv10163903, essv10163887, essv10163917, essv10163922, essv10163895, essv10163859, essv10163926, essv10163941, essv10163881, essv10163945, essv10163874

Samples

NA19222, HG02496, HG03052, HG01359, HG03111, NA18881, NA19020, HG03130, HG03298, HG02476, HG03190, HG03577, HG02589, HG02536, HG03069, HG02769, NA19107, HG03199, NA18519, HG03086, HG03452, NA19198, HG02620, HG02854, NA19197, NA18498, HG01242, HG02505, HG03520, HG01398, HG03556, HG02573, NA19372, HG02642, NA19317, NA19036, HG02427, NA18864, NA20127, NA18908, HG03270, HG02820, HG01187, NA18934, HG03511, HG03547, HG01879, HG03159, HG02537, HG03563, HG03472, HG01311, NA19461, HG03382, HG03476, NA19031, HG02283, HG01130, HG02979, NA19452, NA19160, HG02594, HG03064, NA19017, HG02455, HG03028, HG02282, HG02807, NA19108, NA18517, HG02799, HG02759, NA20276, HG02837, NA18865, HG03127, HG02941, HG03473, HG02580, NA20281, NA19360, NA19117, HG03442, NA19351, HG02053, HG02679, NA18876, HG03077, HG03401, NA19030, NA18488, HG03376, HG03198, HG03303

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3587695

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	94
Observed Complex	0
Frequency	n/a