Variant Details

Variant: esv2675033

Internal ID

9594452

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr15:66414198..66414345	hg38	UCSC Ensembl
	chr15:66706536..66706683	hg19	UCSC Ensembl

Cytoband

15q22.31

Allele length

Assembly	Allele length
hg38	148
hg19	148

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv455e199

Supporting Variants

essv5742339, essv6411652, essv5873710, essv6032870, essv5890370, essv5694181, essv6330336, essv6278982, essv6557103, essv6304975, essv6151967, essv6249184, essv5792588, essv5683682, essv6520264, essv6473672, essv5484551, essv5448027, essv5514503, essv6146403, essv6586687, essv6130190, essv5991774, essv6115397, essv5660364, essv5807307, essv6491289, essv5549074, essv5760081, essv5431704, essv5482860, essv5658779, essv6120090, essv5505774, essv6478900, essv5670276, essv6142869, essv5942040, essv6531271, essv5965777, essv5409774, essv6114333, essv6581576, essv6446861, essv5704544, essv6524385, essv6354243, essv6287823, essv5690389, essv5396695, essv5851867, essv5643957, essv5423859, essv5947435, essv5543804, essv5630884, essv5622179, essv6160858, essv6146028, essv6293284, essv5606035, essv5835562, essv6576242, essv5588007, essv6516337, essv5832138, essv6253381, essv6590623, essv6435393, essv5973271, essv6367582, essv6505377, essv6271845, essv5600493, essv6192911, essv5979896, essv5857161, essv5667803, essv5471749, essv5751733, essv5709078, essv6501066, essv6496682, essv5535899, essv6162502, essv6592473, essv5831001, essv6279576, essv6216641, essv5642714, essv5732790, essv6247497, essv5485404, essv6564831, essv6412543, essv6390679, essv6342211, essv6159084, essv5841001, essv6181844, essv5710574, essv6267712, essv5453429, essv6051837, essv6458759, essv6111643, essv6487550, essv6281555, essv5802646, essv6517513, essv6172766, essv5603044, essv6081463, essv6214937, essv6360590, essv6552903, essv5520078, essv6318685, essv5755817, essv5816454, essv5676842, essv5432983, essv5717168, essv5968480, essv6053895, essv6197179, essv6538952, essv6439902, essv5990901, essv6497685, essv6078342, essv5635347, essv6326407, essv6376430, essv6083677, essv6172118, essv5705713, essv5583676, essv5435801, essv6378703, essv6190372, essv6315683, essv5609707, essv6090054, essv6020352, essv5812519, essv6011960, essv5588935

Samples

NA11830, NA18924, NA19909, NA11829, NA18592, NA10851, HG00100, NA11931, HG01374, HG01066, HG00306, NA18999, NA20512, NA12045, HG00318, NA18486, NA19819, NA18596, NA18959, HG00737, HG01518, HG01051, HG00261, NA12399, NA12155, HG01522, NA12341, HG00327, NA18967, HG01250, NA19660, NA19005, NA18944, NA18489, HG01351, NA19723, NA12891, NA12348, HG01492, NA07048, NA19054, HG00270, NA19782, HG00120, HG00148, HG00106, HG00156, NA20812, HG01495, NA19719, NA19372, HG00422, NA12889, NA20811, NA19189, HG01198, HG00159, NA19239, HG01048, HG01133, NA20342, HG00178, NA18867, HG00253, NA20515, NA19921, HG00264, NA11831, HG00543, HG00313, HG01136, HG00154, NA19908, NA12489, HG00266, HG01187, HG00145, HG00328, NA12878, NA20810, NA20536, HG00533, HG00263, HG00275, NA18579, NA20519, NA18630, NA18907, NA18537, HG01390, NA20525, NA18566, NA11919, HG00651, NA12249, NA19750, NA12892, HG00613, NA19009, NA18555, HG00146, HG00704, NA19225, NA12778, HG00126, HG01204, NA19012, NA18576, NA12043, NA18953, NA19003, HG00258, NA20799, NA18542, NA20801, NA18533, NA12716, NA19749, HG00366, HG00357, NA18941, HG00098, HG01375, NA19835, HG00607, HG00116, NA20803, NA20797, NA18610, NA12347, NA20341, HG01491, HG00312, NA20582, HG00267, HG01254, NA20510, NA18873, NA11843, NA18983, NA07056, HG01111, NA19758, NA18624, NA19463, NA07000, NA12154, NA12776

Known Genes

MAP2K1

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2675033

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	148
Observed Complex	0
Frequency	n/a