Variant Details

Variant: esv2668480

Internal ID

9587899

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:11854051..11855011	hg38	UCSC Ensembl
	chr11:11875598..11876558	hg19	UCSC Ensembl

Cytoband

11p15.3

Allele length

Assembly	Allele length
hg38	961
hg19	961

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5783568, essv5834092, essv5621059, essv5936834, essv5898182, essv6328502, essv6596336, essv5756833, essv5471701, essv5813404, essv5617976, essv6454812, essv6164130, essv5569038, essv6516836, essv6412774, essv6401089, essv6167494, essv6343586, essv6072495, essv5799952, essv6519582, essv6446122, essv6008064, essv5985141, essv6114936, essv5444572, essv6458056, essv6444912, essv6433232, essv6077528, essv6187896, essv6285466, essv6248986, essv5933174, essv6079036, essv5812484, essv6009349, essv5682247, essv6111038, essv6301220, essv6537150, essv6405545, essv6551963, essv6521085, essv5978466, essv6191268, essv6428009, essv6559886, essv5909624, essv6014055, essv5415004, essv5946327, essv6597009, essv6231691, essv5932255, essv5679091, essv5404228, essv5659665, essv6520039, essv5465958, essv6556936, essv5430297, essv6051907, essv6225136, essv6512764, essv5770388, essv5747367, essv5970440, essv5679767, essv6215823, essv5486162, essv6073878, essv5511135, essv6444678, essv5428976, essv5927677, essv6046456, essv6215414, essv6095293, essv6027740, essv5901381, essv6581754, essv6074314, essv6172643, essv5900194, essv5539785, essv6387000, essv5422693, essv6055776, essv5647053, essv6318322, essv5927867, essv5660988, essv6395913, essv5779356, essv6446085, essv6082388, essv5733820, essv5823138, essv6187055, essv6534123, essv5552837, essv5578034, essv6035102, essv5434771, essv5768858, essv5762122, essv5459581, essv5437551, essv5651920, essv5406769, essv5637058, essv6219741, essv6393849, essv5884690, essv6486605, essv6504145, essv6296218, essv5981769, essv6570999, essv6117230, essv6167195, essv6188167, essv5701890, essv5858692, essv5947944, essv6467647, essv5765596, essv5450764, essv6133840, essv6348195, essv5551439, essv5863470, essv5515601, essv6395151, essv6342292, essv6040324, essv5919796, essv6562276, essv6417181, essv6234652, essv5496887, essv6054110, essv6274215, essv5923516, essv5632931, essv5999456, essv6390567, essv5645989

Samples

HG00626, HG00189, HG00592, HG01098, HG00143, HG00608, NA18621, NA12286, HG00671, NA18592, HG01359, NA20813, HG00640, HG01465, HG00699, NA20805, HG00566, NA20808, HG00177, NA12399, HG00271, HG00663, NA07346, NA18563, HG00641, HG00138, NA19660, NA19076, NA19005, HG00589, HG00272, HG00122, HG01488, HG00330, NA20769, HG00610, NA18574, NA20768, NA19088, HG00270, NA20513, NA18964, HG01134, HG00277, NA12275, HG01455, NA19651, HG00106, NA20819, HG01170, HG00262, NA19087, HG00309, NA18990, HG01198, HG00159, HG01048, HG00178, NA20757, HG00253, NA20755, NA20753, HG01124, NA19007, HG00313, HG00137, HG01183, HG00149, NA19082, NA19707, HG00557, HG00732, HG00436, HG00583, NA19081, NA18579, NA20126, HG00692, HG00635, HG01390, HG01047, HG00324, HG01073, HG00273, HG00651, HG00404, HG00331, NA20538, HG01101, NA19059, HG01334, NA18555, NA19452, NA18963, NA20542, NA19625, NA18634, NA12546, NA20534, NA18541, NA18546, NA20296, NA19685, HG00258, HG00119, NA18535, HG00336, NA18543, NA18559, HG00353, HG00375, HG00357, NA19773, HG01174, NA20778, HG01113, HG01137, NA20281, HG00662, HG00418, NA19085, NA18610, HG01489, HG00620, HG00339, NA20341, NA19759, NA19398, NA19078, HG00513, HG00578, HG00312, HG00259, NA19060, HG00656, HG00342, NA18636, HG00131, NA19080, HG00252, HG00595, NA18984, HG00472, NA19004, HG00171, NA19063, NA19346, NA19074, HG00437, HG00581

Known Genes

USP47

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)

esv2668480

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	150
Observed Complex	0
Frequency	n/a