Variant Details

Variant: esv2661922

Internal ID

9928027

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr22:23683430..23685351	hg38	UCSC Ensembl
	chr22:24025617..24027538	hg19	UCSC Ensembl

Cytoband

22q11.23

Allele length

Assembly	Allele length
hg38	1922
hg19	1922

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6252672, essv5619186, essv5957878, essv6529668, essv6425213, essv6538136, essv6086806, essv5531148, essv6390414, essv5896499, essv5977937, essv5791694, essv5507782, essv6554695, essv5897314, essv5876190, essv5407951, essv6160208, essv5893932, essv5624126, essv6420902, essv5677095, essv6280010, essv6201402, essv5735937, essv6326088, essv5686369, essv5440152, essv5754335, essv6355162, essv6170130, essv6166966, essv6110015, essv5748949, essv5724010, essv5602022, essv6527472, essv5411123, essv5920395, essv5633281, essv5501512, essv5465221, essv5409239, essv6259815, essv6187046, essv6279256, essv6054787, essv5632726, essv5754633, essv6574171, essv6523837, essv5868486, essv5572085, essv6087074, essv5489522, essv6056362, essv5721339, essv5602940, essv6420491, essv6028563, essv6580769, essv6045005, essv6560366, essv6039978, essv5760405, essv6145741, essv6347098, essv5834664, essv6053950, essv6509168, essv6488872, essv5934759, essv5888994, essv5962162, essv6222680, essv5926146, essv5709649, essv5922980, essv6570363, essv5621197, essv6265187, essv6277860, essv5776049, essv6506817, essv5664606, essv5618213, essv5500947, essv6589131, essv6035766, essv6513821, essv5438112, essv6274968, essv6568203, essv6347442, essv6036547, essv5789682, essv6182009, essv5761139, essv5533424, essv5960029, essv6504043, essv6094788, essv5797693, essv6127821, essv5720903, essv5917586, essv6484994, essv5978948, essv6202655, essv6430813, essv5776343, essv6016040, essv6462501, essv5929659, essv6319663, essv6161441, essv5681192, essv6428665, essv6420637, essv5737111, essv5592778, essv6204928, essv5517753, essv6422282, essv6269733, essv5557832, essv6244513, essv5587432, essv6172175, essv5524258, essv6541119, essv5825917, essv5731536, essv5679582, essv6288445, essv5885686, essv5878873, essv5650350, essv6216351

Samples

HG00096, NA19394, NA18502, HG01173, NA19058, HG01521, NA20543, NA20508, NA11829, HG00361, NA10851, NA20531, NA11931, HG01066, HG00315, HG00151, NA20816, NA18999, HG00640, NA18870, NA12400, HG01051, NA20771, NA12750, NA07357, HG01140, NA12413, NA12341, HG00327, NA20814, HG00138, NA19379, NA19201, NA18527, NA19315, NA19448, HG01488, NA20756, NA19198, HG00330, NA12348, HG01492, NA07048, NA07347, NA12283, NA20540, NA20513, NA19782, NA19130, NA18949, NA12761, NA11930, HG00281, HG00139, NA20539, HG01080, NA20518, NA20278, NA20775, NA12156, HG00262, HG01072, NA19471, NA12889, HG00309, HG00160, HG01198, HG00338, HG01133, NA19445, HG00326, NA18908, HG00253, HG00739, NA11993, HG00108, NA11831, NA10847, HG00133, HG00149, NA12489, HG00731, NA20800, NA20524, HG00245, NA18956, NA12718, NA12234, HG01073, NA12829, NA19750, HG00117, HG00157, NA18963, NA12144, NA06985, NA20828, HG00246, HG00126, NA20542, NA12546, HG01107, NA20534, NA18953, HG00124, HG01190, HG00285, HG00265, NA19256, NA18517, NA19712, NA12272, NA19435, NA07051, NA20785, NA20790, NA20530, HG01375, NA20778, NA20504, HG01137, NA07037, HG00339, NA19759, NA06994, HG01055, NA20510, NA20786, NA20807, NA11843, NA18983, NA18488, NA20585, NA18522, NA12154, HG01097, NA18612, NA18487, NA20772

Known Genes

GUSBP11

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)

esv2661922

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	139
Observed Complex	0
Frequency	n/a