Variant Details

Variant: esv2667751

Internal ID

9933856

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr9:130268363..130272522	hg38	UCSC Ensembl
	chr9:133030642..133034801	hg19	UCSC Ensembl

Cytoband

9q34.11

Allele length

Assembly	Allele length
hg38	4160
hg19	4160

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5853859, essv5565967, essv5985612, essv6359289, essv6348371, essv5644914, essv6239815, essv5998416, essv6465368, essv6151309, essv6293877, essv5833066, essv5900005, essv5933000, essv6178887, essv5965225, essv5523804, essv6349988, essv6052303, essv5662335, essv6390262, essv6099986, essv6434795, essv6328102, essv5883870, essv6172445, essv6535000, essv6065840, essv5894121, essv5498912, essv5601437, essv6004095, essv6522617, essv6514986, essv5961951, essv6194857, essv6379210, essv5848199, essv6025263, essv5759591, essv6158672, essv5665464, essv6518503, essv5868526, essv5690366, essv5611507, essv5997073, essv6445760, essv6563330, essv6210110, essv6555643, essv5970224, essv6437113, essv6581010, essv5840956, essv6090196, essv5873113, essv6133709, essv6349184, essv5699673, essv6473883, essv6265134, essv5719080, essv6180632, essv5766906, essv5787577, essv6424035, essv5824482, essv5459908, essv5901597, essv6448444, essv5813172, essv6155491, essv5674772, essv6542137, essv5859789, essv5610926, essv6002160, essv5863331, essv6245328, essv5797428, essv5993514, essv6036989, essv5937518, essv5561085, essv5677710, essv5421690, essv6065486, essv5486424, essv6520248, essv6113635, essv5455938, essv5982062, essv6111040, essv6134402, essv5867000, essv6096156, essv5785289, essv5745580, essv5427862, essv6511099, essv5551385, essv5442450, essv5459639, essv6289603, essv6523548, essv6271916, essv5454232, essv6302529, essv6516842, essv5858952, essv5738152, essv5636095, essv6018945, essv6553497, essv5520286, essv5489625, essv5944685, essv6368458, essv6333115, essv5609422

Samples

HG00189, NA12717, HG00231, NA11995, HG00361, NA12273, NA12414, NA18599, HG00306, NA20813, HG00233, NA20512, HG00244, HG00103, NA18959, HG00177, NA12400, NA20771, NA20806, NA12341, HG00337, HG00271, NA18940, HG01366, HG00122, HG01351, NA12891, NA07048, NA11918, NA07347, NA12283, NA20540, NA12287, HG00369, NA20287, HG00311, HG00243, HG00158, NA12761, HG00277, NA19651, HG01067, HG00148, NA20819, NA20775, HG00325, NA11932, NA11994, HG00118, HG01133, NA20342, HG00178, NA20757, HG01550, HG00108, NA11831, HG01136, HG00149, NA12489, NA20800, HG00268, HG00380, NA19670, NA12878, NA20809, NA19455, HG00533, HG00275, NA20506, NA12718, NA18572, NA18548, NA18537, HG00324, NA19774, NA19655, HG00373, NA11893, NA20538, NA12892, NA06989, HG00140, NA12546, HG01107, NA19675, NA18945, NA12043, NA20773, NA20522, NA19652, NA20801, HG00336, NA18564, HG00366, HG00375, HG00357, NA12272, NA07051, NA12046, NA20790, HG01375, HG00308, HG00237, NA19679, HG00319, NA20516, HG00339, HG01491, HG00312, NA19779, HG00174, NA20510, NA12830, NA19726, NA19780, HG00377, HG00372, HG00274, HG00171, HG01112, HG01191

Known Genes

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)

esv2667751

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	121
Observed Complex	0
Frequency	n/a