Variant Details

Variant: esv3647708

Internal ID

7034448

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr22:37348297..37354097	hg38	UCSC Ensembl
Inner	chr22:37348297..37354097	hg38	UCSC Ensembl
Outer	chr22:37348208..37354321	hg38	UCSC Ensembl
	chr22:37744338..37750137	hg19	UCSC Ensembl
Inner	chr22:37744338..37750137	hg19	UCSC Ensembl
Outer	chr22:37744249..37750361	hg19	UCSC Ensembl

Cytoband

22q13.1

Allele length

Assembly	Allele length
hg38	5801
hg19	5800

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv16421043, essv16421037, essv16421026, essv16421013, essv16420984, essv16421030, essv16421058, essv16421021, essv16420993, essv16420999, essv16421036, essv16421004, essv16420988, essv16421046, essv16421032, essv16421022, essv16420998, essv16420991, essv16421005, essv16421018, essv16420987, essv16421049, essv16421041, essv16421056, essv16421068, essv16421017, essv16421044, essv16420982, essv16421034, essv16421025, essv16421050, essv16421066, essv16421040, essv16421060, essv16421054, essv16420990, essv16420992, essv16420983, essv16421020, essv16421023, essv16421057, essv16420981, essv16421000, essv16421019, essv16420995, essv16421002, essv16421027, essv16421003, essv16421008, essv16421047, essv16421055, essv16421038, essv16421011, essv16421069, essv16421065, essv16420989, essv16421059, essv16420980, essv16421063, essv16421035, essv16421033, essv16421051, essv16421007, essv16421001, essv16421062, essv16421014, essv16421010, essv16420996, essv16421053, essv16421028, essv16420994, essv16421067, essv16421009, essv16421052, essv16421016, essv16421061, essv16421031, essv16420985, essv16421012, essv16421015, essv16421039, essv16421029, essv16421042, essv16421006, essv16421064, essv16421048, essv16420997, essv16421024, essv16421045, essv16420986

Samples

NA20762, HG00384, HG00361, HG00242, NA12273, HG01389, HG00181, HG01632, NA07357, HG01694, HG01070, HG00109, HG01177, NA19678, HG00238, NA11918, HG01354, NA19681, NA12282, HG01080, HG00379, NA11932, HG00232, HG00309, NA19725, HG00159, HG01048, HG00178, HG00739, HG01124, HG00313, HG00137, HG01784, HG00188, NA19657, HG00380, HG02233, NA20787, HG00145, HG02334, HG01790, HG01789, HG00190, NA20760, HG00132, HG01768, HG00344, HG01345, NA20519, HG02508, HG00239, HG01047, HG01392, HG00350, NA11840, NA12249, NA19752, NA20282, HG01474, HG00276, NA06985, HG00246, HG01148, NA20872, HG00382, NA20801, HG01190, HG02010, HG00353, HG02220, NA12873, HG02232, NA07037, NA12347, HG00339, HG01606, HG01765, HG01432, HG03863, NA20289, HG00186, HG01631, HG01105, HG01479, NA19758, HG00171, NA12006, NA20585, HG00362, HG00255

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3647708

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	90
Observed Complex	0
Frequency	n/a