Variant Details

Variant: esv3421146

Internal ID

15268104

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:32412722..32412734	hg38	UCSC Ensembl
Inner	chr11:32412713..32412743	hg38	UCSC Ensembl
Outer	chr11:32412701..32412752	hg38	UCSC Ensembl
	chr11:32434268..32434280	hg19	UCSC Ensembl
Inner	chr11:32434259..32434289	hg19	UCSC Ensembl
Outer	chr11:32434247..32434298	hg19	UCSC Ensembl
	chr11:32390844..32390856	hg18	UCSC Ensembl
Inner	chr11:32390865..32390835	hg18	UCSC Ensembl
Outer	chr11:32390823..32390874	hg18	UCSC Ensembl

Cytoband

11p13

Allele length

Assembly	Allele length
hg38	289
hg19	289
hg18	289

Variant Type

CNV insertion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv8952261, essv8952285, essv8952312, essv8952257, essv8952299, essv8952263, essv8952267, essv8952266, essv8952318, essv8952258, essv8952306, essv8952259, essv8952254, essv8952317, essv8952255, essv8952278, essv8952250, essv8952276, essv8952311, essv8952252, essv8952279, essv8952301, essv8952305, essv8952270, essv8952286, essv8952300, essv8952295, essv8952275, essv8952289, essv8952298, essv8952246, essv8952274, essv8952245, essv8952284, essv8952269, essv8952265, essv8952280, essv8952272, essv8952302, essv8952292, essv8952303, essv8952296, essv8952307, essv8952247, essv8952248, essv8952291, essv8952253, essv8952281, essv8952288, essv8952297, essv8952310, essv8952316, essv8952268, essv8952309, essv8952314, essv8952277, essv8952308, essv8952251, essv8952256, essv8952294, essv8952283, essv8952264, essv8952313, essv8952287, essv8952290, essv8952273, essv8952262

Samples

NA18502, NA18947, NA18861, NA18592, NA18561, NA18603, NA12045, NA18545, NA12004, NA18504, NA18959, NA18526, NA12750, NA07346, NA18563, NA18944, NA18940, NA18550, NA18489, NA18558, NA18547, NA18960, NA18942, NA11918, NA18571, NA18498, NA18964, NA18949, NA12761, NA18638, NA11831, NA18605, NA18956, NA18516, NA18579, NA18572, NA18948, NA18907, NA18566, NA18573, NA19114, NA18499, NA12249, NA18912, NA18532, NA19099, NA19257, NA18555, NA12144, NA18593, NA18576, NA18608, NA19108, NA18961, NA18952, NA18517, NA18943, NA18501, NA19093, NA18609, NA18552, NA19129, NA18522, NA12154, NA18562, NA18965, NA18577

Known Genes

WT1

Method

Sequencing

Analysis

Platform

Illumina

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3421146

Frequency

Sample Size	185
Observed Gain	67
Observed Loss	0
Observed Complex	0
Frequency	n/a