Variant Details

Variant: esv3635113

Internal ID

7021913

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr14:82737585..82740517	hg38	UCSC Ensembl
Inner	chr14:82737586..82740517	hg38	UCSC Ensembl
Outer	chr14:82737585..82740518	hg38	UCSC Ensembl
	chr14:83203929..83206861	hg19	UCSC Ensembl
Inner	chr14:83203930..83206861	hg19	UCSC Ensembl
Outer	chr14:83203929..83206862	hg19	UCSC Ensembl

Cytoband

14q31.1

Allele length

Assembly	Allele length
hg38	2933
hg19	2933

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv15082964, essv15082938, essv15082982, essv15082959, essv15082977, essv15082970, essv15082937, essv15082981, essv15082972, essv15082914, essv15082922, essv15082934, essv15082976, essv15082967, essv15082916, essv15082910, essv15082983, essv15082929, essv15082947, essv15082957, essv15082961, essv15082919, essv15082918, essv15082925, essv15082984, essv15082973, essv15082921, essv15082932, essv15082975, essv15082945, essv15082980, essv15082962, essv15082955, essv15082915, essv15082928, essv15082935, essv15082965, essv15082936, essv15082951, essv15082931, essv15082913, essv15082953, essv15082909, essv15082924, essv15082940, essv15082927, essv15082971, essv15082963, essv15082979, essv15082923, essv15082912, essv15082966, essv15082952, essv15082960, essv15082942, essv15082974, essv15082950, essv15082941, essv15082933, essv15082943, essv15082926, essv15082920, essv15082968, essv15082946, essv15082969, essv15082949, essv15082958, essv15082954, essv15082917, essv15082944, essv15082948, essv15082911, essv15082956, essv15082908, essv15082939, essv15082978, essv15082930

Samples

NA18745, NA18647, NA18592, HG00524, HG00766, HG01802, NA18625, NA18616, HG02040, HG00449, HG02154, NA19089, HG02185, HG02140, HG00689, NA18567, NA18993, HG03604, HG02130, NA18582, NA19054, HG00451, HG02067, HG02389, HG00422, NA18986, NA18966, NA18990, HG01844, NA18640, NA18973, HG00530, HG02134, HG00464, NA18544, NA18605, NA19082, HG00982, NA19070, NA18525, HG02142, HG00556, HG01810, HG00584, NA18579, NA18948, HG01852, NA18630, NA19000, HG00690, HG00684, NA19001, HG00525, NA18555, NA18593, HG02408, HG02127, NA18541, NA18952, NA18628, NA18941, HG00473, NA18591, NA18943, HG00662, NA18610, HG02398, HG00707, NA18971, NA18987, HG00595, HG01807, NA18989, NA18740, NA18622, HG00437, NA18577

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3635113

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	77
Observed Complex	0
Frequency	n/a