Variant Details

Variant: esv2670295

Internal ID

9936400

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr3:114938105..114949754	hg38	UCSC Ensembl
	chr3:114656952..114668601	hg19	UCSC Ensembl

Cytoband

3q13.31

Allele length

Assembly	Allele length
hg38	11650
hg19	11650

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv881e199

Supporting Variants

essv6522941, essv5914602, essv6064083, essv6034865, essv6193926, essv5911497, essv5404940, essv6146527, essv6441899, essv5462679, essv5522542, essv5620714, essv6542309, essv6258614, essv5735460, essv6265017, essv6009848, essv6421178, essv5822624, essv6415999, essv6081388, essv6535665, essv5546549, essv5655880, essv5923574, essv5792454, essv6060842, essv6032431, essv6080624, essv6544132, essv6533360, essv5720963, essv5798797, essv6031270, essv5871998, essv5922074, essv5790319, essv6004621, essv5597788, essv6127446, essv6276939, essv6596647, essv6491690, essv6035507, essv5997426, essv6073948, essv5539593, essv5562213, essv5626636, essv6008992, essv5635284, essv6177056, essv6460724, essv6104322, essv6487011, essv6358134, essv5570534, essv6316724, essv6492168, essv6183648, essv5781953, essv6477744, essv5570511, essv5553520, essv6153826, essv6285650, essv6314402, essv6319381, essv5830002, essv5698890, essv5698588, essv6217974, essv5537688, essv5593155, essv6247937, essv6267901, essv5721756, essv6476409, essv6429583, essv5512643, essv6194140, essv5694378, essv6325631, essv5625646, essv6354354, essv6058138, essv6264179, essv6227075, essv5520871, essv5817160, essv5439875, essv5552760, essv5490275, essv5885961, essv5672847, essv6514117, essv5821489, essv5846105, essv5959656, essv6153712, essv6276416, essv6056050, essv5651020, essv6150940, essv6551697, essv6106201, essv5425598, essv6037837, essv6277353, essv6371685, essv5693875, essv6522302, essv5887784, essv5952089, essv5633786, essv6289767, essv6306571, essv5446812

Samples

HG01356, NA19703, NA18924, NA19466, NA19204, NA19399, NA19332, HG01079, NA18507, NA19350, NA18486, NA19819, NA19393, NA18504, NA20332, HG01461, NA19098, NA18870, NA19920, NA18510, NA19446, NA19396, NA19171, NA19379, NA19319, NA19201, NA18489, NA19678, NA18923, NA19198, NA18619, NA19916, NA19131, NA19197, NA19313, NA19138, NA18498, NA19130, NA18874, NA19137, NA19372, NA19371, NA19385, NA19317, NA19159, NA19901, NA18520, NA19239, HG01048, NA19209, NA19921, NA19451, HG01183, NA19210, NA19437, NA19707, NA18934, NA19462, NA19347, NA19152, NA19455, NA19236, NA18516, NA19982, NA18910, NA18871, HG01047, HG01102, NA19461, NA19114, NA11919, NA18499, NA19099, NA19338, NA19257, NA19225, NA19160, HG01107, NA19436, NA19401, NA19390, NA19834, NA19108, NA19256, NA19147, NA18517, NA20276, NA19712, NA19434, NA19747, HG00734, HG00638, NA19444, NA19380, NA19144, NA19835, NA19334, NA19470, NA19311, NA19360, NA19078, NA18501, NA19248, NA19472, NA19223, NA19474, NA19093, NA18636, NA19102, NA18873, NA19116, NA19213, NA19900, NA19430, NA18505, NA19463, NA18511, NA18487

Known Genes

ZBTB20

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2670295

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	118
Observed Complex	0
Frequency	n/a