Variant Details

Variant: esv2672903

Internal ID

9939008

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:56640464..56640781	hg38	UCSC Ensembl
	chr11:56407940..56408257	hg19	UCSC Ensembl

Cytoband

11q12.1

Allele length

Assembly	Allele length
hg38	318
hg19	318

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6266877, essv6009158, essv5405176, essv6324254, essv6192199, essv6423693, essv5837722, essv6562915, essv5541911, essv6540178, essv6206371, essv6216163, essv6343893, essv6435813, essv6065696, essv5708175, essv6320302, essv6250706, essv5594452, essv6521130, essv5998653, essv5943918, essv5739048, essv6215711, essv6316794, essv6146372, essv6203628, essv6413544, essv6188114, essv6233498, essv6082597, essv5870476, essv6280875, essv6569629, essv6532991, essv5894784, essv5849217, essv5613907, essv5410393, essv6299843, essv6241929, essv5726011, essv5886568, essv5937392, essv5467158, essv5833687, essv6400621, essv6097742, essv6430265, essv5635055, essv6107963, essv6380387, essv6152894, essv6212097, essv6033643, essv6241381, essv6291309, essv5748188, essv5709568, essv5729497, essv6190174, essv6532292, essv6147444, essv5952636, essv6516254, essv6089642, essv6482774, essv6377203, essv6087883, essv6388807, essv6395297, essv6137416, essv5598695, essv6498387, essv6509384, essv5663227, essv6379738, essv6264455, essv6049715, essv6518365, essv5604073, essv6257910, essv6005938, essv5971898, essv5702030, essv5916221, essv5567223, essv5904509, essv5967535, essv6121867, essv6130539, essv5691769, essv5699041, essv6473048, essv6532916, essv5656812, essv6428319, essv5567353, essv5673114, essv6218308, essv5587790, essv5446257, essv6072909, essv6369954, essv6248403, essv6216571, essv5472409, essv6503196, essv6038259, essv6539784, essv6419883, essv5660417, essv6283997, essv6335654, essv5547903, essv6548001, essv5618336, essv5697452, essv5914886, essv5892297, essv5810450, essv6203453, essv6264558, essv6232931, essv5775010, essv5761033, essv6218820, essv6023936, essv5723313

Samples

NA12383, NA18502, HG01060, HG01441, NA12717, NA18924, NA11829, NA19204, NA18861, NA18508, NA10851, NA20783, NA11920, HG00315, NA20813, NA18917, NA12045, NA18486, NA18504, NA20808, HG00150, NA19190, NA19098, NA18870, NA18510, NA07357, HG00327, NA18519, NA18489, NA19119, NA18923, NA19131, NA18916, NA19197, NA20540, NA19138, NA18498, NA19130, HG00139, NA19720, NA19651, HG01067, NA18874, NA12156, NA18868, HG00325, NA11932, NA19207, NA19172, HG00182, HG00160, NA19189, NA18520, NA19209, HG00326, NA18908, HG00323, NA20755, NA19200, NA19247, HG00268, HG00176, NA18934, HG01384, NA19152, NA18933, NA18516, NA18910, NA18871, HG01149, NA18907, NA20525, NA19654, HG00273, NA19114, NA12829, HG00331, NA18499, NA18856, NA18912, NA18853, NA19099, NA19257, NA19225, NA18523, NA19160, NA18858, NA20773, NA19652, NA18909, NA19108, NA19147, NA18517, HG00278, NA19144, NA20785, NA12046, HG01494, NA19439, NA20544, HG01137, NA12763, HG00339, HG00125, NA20341, NA18501, NA19248, HG00259, HG00329, HG00342, NA19093, HG00310, HG00186, NA19102, NA18873, HG00112, NA20807, HG00131, NA19213, HG00274, NA07056, NA18505, NA19129, NA19758, NA12890, NA18511, NA18522, NA19346, NA18487

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2672903

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	129
Observed Complex	0
Frequency	n/a