Variant Details

Variant: esv2669391

Internal ID

9935496

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr9:85413841..85415374	hg38	UCSC Ensembl
	chr9:88028756..88030289	hg19	UCSC Ensembl

Cytoband

9q21.33

Allele length

Assembly	Allele length
hg38	1534
hg19	1534

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6136835, essv6156781, essv5629598, essv5447988, essv6032255, essv6372653, essv6204066, essv6409536, essv5410074, essv5938005, essv5593996, essv5972975, essv6070753, essv5697530, essv5433874, essv6014904, essv5962371, essv5703848, essv6353267, essv5531277, essv6193349, essv6183752, essv5790696, essv6462459, essv6572185, essv6521225, essv6075765, essv5474108, essv6458185, essv5449120, essv5582134, essv5543664, essv5409973, essv6242411, essv6098064, essv6540788, essv5879477, essv6563676, essv5790332, essv5420716, essv6036287, essv5694067, essv5671346, essv6358630, essv5946226, essv5542685, essv6259057, essv6215213, essv5519989, essv5470520, essv6477729, essv6419853, essv5427911, essv6166983, essv6540854, essv6331857, essv6246226, essv6485123

Samples

HG00096, NA18924, NA11933, HG00151, NA18603, NA18486, NA19920, NA18633, NA12155, NA19005, HG00689, HG00448, NA19771, HG01134, HG00281, HG00683, NA18977, HG00325, NA19917, NA12889, NA19722, NA20811, HG00637, NA12748, NA19908, HG00443, NA19347, HG00653, NA18991, NA19982, HG00500, HG00619, NA19338, HG00704, HG00258, NA18632, NA19652, HG00155, NA19390, NA19712, HG00366, NA19835, NA18943, NA18615, NA18631, NA19472, HG00329, NA19713, HG00123, NA20510, NA12830, HG00310, HG00186, NA19770, NA19213, NA18624, HG01191, NA19346

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)

esv2669391

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	58
Observed Complex	0
Frequency	n/a