Variant Details

Variant: esv3600314

Internal ID

6987358

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr4:40633581..40635163	hg38	UCSC Ensembl
Inner	chr4:40633621..40635123	hg38	UCSC Ensembl
Outer	chr4:40633541..40635203	hg38	UCSC Ensembl
	chr4:40635598..40637180	hg19	UCSC Ensembl
Inner	chr4:40635638..40637140	hg19	UCSC Ensembl
Outer	chr4:40635558..40637220	hg19	UCSC Ensembl

Cytoband

4p14

Allele length

Assembly	Allele length
hg38	1583
hg19	1583

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv11404784, essv11404760, essv11404789, essv11404785, essv11404763, essv11404777, essv11404776, essv11404754, essv11404779, essv11404755, essv11404750, essv11404753, essv11404781, essv11404762, essv11404786, essv11404775, essv11404758, essv11404773, essv11404765, essv11404764, essv11404766, essv11404772, essv11404747, essv11404767, essv11404780, essv11404751, essv11404761, essv11404746, essv11404748, essv11404793, essv11404749, essv11404756, essv11404752, essv11404757, essv11404771, essv11404791, essv11404770, essv11404782, essv11404768, essv11404774, essv11404794, essv11404788, essv11404759, essv11404783, essv11404778, essv11404787, essv11404790, essv11404792, essv11404769

Samples

HG01985, HG03096, HG02798, HG03295, HG02589, HG03372, NA19374, HG03385, NA18923, HG02620, NA18916, NA19138, HG03479, HG03224, HG02816, HG02922, HG02281, HG02278, HG03209, HG02703, HG02573, NA19239, NA19025, HG03583, HG02477, NA19200, NA19027, HG02820, HG01171, HG03088, HG02678, HG02968, HG03301, HG02577, HG02772, NA19206, HG02667, HG02557, NA19390, HG02799, NA19473, HG03433, HG01342, NA19117, NA19248, NA19351, NA19102, HG02052, HG03271

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3600314

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	49
Observed Complex	0
Frequency	n/a