Variant Details

Variant: esv2667872

Internal ID

9933977

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr1:224945928..225060952	hg38	UCSC Ensembl
	chr1:225133630..225248654	hg19	UCSC Ensembl

Cytoband

1q42.12

Allele length

Assembly	Allele length
hg38	115025
hg19	115025

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv101e199

Supporting Variants

essv6584682, essv5721501, essv6573202, essv5636613, essv6049412, essv5805566, essv5790938, essv6586025, essv5499454, essv6196659, essv6064892, essv5966840, essv5766163, essv5654572, essv6159360, essv6587150, essv5949792, essv5592607, essv6167399, essv5492960, essv6044684, essv5787696, essv6533770, essv6383572, essv5495847, essv6456180, essv6150808, essv5629945, essv5696786, essv5434678, essv6380461, essv5460870, essv5539990, essv6142250, essv5928187, essv5553580, essv6240323, essv5535606, essv5471691, essv5937086, essv5732151, essv6493713, essv5424512, essv5402873, essv5494373, essv6417464, essv6474677, essv6585757, essv5873437, essv6211318, essv6060545, essv5875344, essv5525227, essv6205998, essv6409700, essv5449735, essv6502143, essv6195992, essv5833018, essv6100879, essv5711529, essv5879279, essv6541086, essv6265066, essv6079817, essv6336092, essv6108987, essv6189790, essv5967119, essv6385173, essv6064422, essv5614078, essv6580168, essv6075043, essv5929752, essv6018428, essv5570949, essv5727239, essv5975922, essv5629427, essv5670128, essv5925398, essv6196195, essv5565883, essv6336369, essv5988217, essv5515092, essv6568522, essv5932494, essv6047662, essv6589388, essv5874806, essv6459862, essv6403990, essv5601743, essv6542896, essv5518385, essv6181852, essv5562143, essv6396961, essv5994265, essv6460021, essv6400585, essv5751648, essv5697257, essv5901805, essv6306827, essv5786346, essv5971080, essv5950298, essv5452865, essv6556311, essv5977872, essv5516630, essv6031693, essv5429998, essv6377092, essv6202757, essv6049917, essv6088273, essv5896775, essv5706687, essv5638858, essv5420005, essv6513504, essv6344603, essv6058943, essv6446566, essv6063936, essv5684762, essv6501225, essv5482560, essv5653030, essv5703869, essv5595527, essv6200003, essv6148834, essv5727002, essv6109614, essv5811174, essv6361703, essv6434910, essv5905065, essv5766601, essv5957938, essv6134753, essv5748325

Samples

NA20761, NA11830, NA12842, NA19055, NA20766, NA12286, NA19466, HG01359, NA20783, HG01079, NA18507, NA11920, NA18599, HG01066, NA20816, NA20813, NA18999, NA20802, NA20532, NA12045, NA18545, NA19819, NA19057, NA18596, NA18530, NA18606, NA12400, NA20771, NA12399, NA20806, NA19067, NA18602, NA12413, NA19107, NA07346, NA19076, NA18550, NA18597, HG00702, NA18635, NA20756, NA18567, NA18619, HG01492, NA18942, NA19062, NA18574, NA18582, NA20540, NA19313, NA20513, NA19681, HG00158, NA18611, HG01134, NA12282, HG01067, NA18874, NA20812, NA19075, NA18617, NA19087, NA12889, NA19002, NA20811, NA18990, NA18520, HG01048, NA19445, HG00178, NA18867, NA19007, NA12777, NA19247, NA20800, NA19070, NA20787, NA20505, NA19077, NA20810, NA20760, NA19455, NA18572, NA20770, NA19064, HG00740, NA19084, NA20581, NA12829, NA11893, NA19453, NA19059, NA18555, NA12144, NA20828, NA19625, NA18593, NA12546, NA18632, NA20801, NA19834, NA19434, NA12775, NA19072, NA18950, HG00357, NA20804, NA20785, NA19010, NA20790, NA20530, NA19835, NA20792, NA19439, NA19467, NA20516, NA19083, NA20803, NA18610, HG01489, NA19818, NA19078, HG00614, HG01491, NA18631, NA19472, NA18987, NA12749, NA19713, HG01055, NA19093, NA20786, NA18873, NA20807, NA20758, NA20826, NA18984, NA07056, NA11892, NA19004, HG00345, NA19063, NA18549, NA19074, HG01437, HG00581, NA19431

Known Genes

DNAH14

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2667872

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	147
Observed Complex	0
Frequency	n/a