Variant Details

Variant: esv2665165

Internal ID

9931270

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr18:74773302..74773474	hg38	UCSC Ensembl
	chr18:72485258..72485430	hg19	UCSC Ensembl

Cytoband

18q22.3

Allele length

Assembly	Allele length
hg38	173
hg19	173

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5549351, essv5604491, essv5745543, essv6269482, essv6103474, essv5816232, essv5755396, essv6023096, essv5894996, essv6414371, essv6118544, essv5535133, essv6569639, essv6279544, essv6351056, essv5746616, essv6262992, essv5510866, essv5851722, essv5585374, essv5481103, essv5771588, essv5491676, essv6556878, essv6175005, essv6097010, essv5997554, essv5889647, essv5411528, essv5529400, essv5982369, essv5849645, essv6466946, essv6269590, essv6221376, essv5803407, essv6078526, essv6222308, essv6461126, essv6438573, essv5986526, essv5734569, essv5437046, essv6493433, essv5435242, essv5780636, essv6559305, essv5876447, essv6461027, essv6561948, essv5535557, essv6368722, essv5700246, essv5596749, essv6094467

Samples

HG00650, HG00442, NA19359, NA18486, NA19355, NA20346, NA19443, NA19396, HG01350, HG01366, HG00251, HG01351, HG01488, NA11918, NA19138, HG01365, NA19384, HG00537, HG00590, NA19404, HG01069, HG01080, NA20278, HG01170, HG01072, NA19372, NA19172, NA18520, HG00326, HG00464, NA19403, NA12003, NA19391, HG00556, NA18871, HG00324, HG00690, NA18499, NA19750, HG01101, HG00276, NA19375, HG00254, NA19390, NA20276, NA19311, HG01108, NA19398, HG00707, HG00672, NA19102, HG00274, HG00472, NA07056, HG01082

Known Genes

ZNF407

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2665165

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	55
Observed Complex	0
Frequency	n/a