Variant Details

Variant: esv3633821

Internal ID

7020627

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr14:25142235..25144515	hg38	UCSC Ensembl
Inner	chr14:25142235..25144515	hg38	UCSC Ensembl
Outer	chr14:25142147..25144625	hg38	UCSC Ensembl
	chr14:25611441..25613721	hg19	UCSC Ensembl
Inner	chr14:25611441..25613721	hg19	UCSC Ensembl
Outer	chr14:25611353..25613831	hg19	UCSC Ensembl

Cytoband

14q12

Allele length

Assembly	Allele length
hg38	2281
hg19	2281

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv14944561, essv14944625, essv14944586, essv14944624, essv14944605, essv14944555, essv14944538, essv14944602, essv14944571, essv14944544, essv14944607, essv14944576, essv14944582, essv14944618, essv14944612, essv14944606, essv14944554, essv14944543, essv14944622, essv14944560, essv14944598, essv14944604, essv14944611, essv14944621, essv14944597, essv14944537, essv14944553, essv14944541, essv14944564, essv14944575, essv14944593, essv14944577, essv14944563, essv14944542, essv14944565, essv14944557, essv14944594, essv14944615, essv14944613, essv14944566, essv14944579, essv14944591, essv14944558, essv14944584, essv14944545, essv14944567, essv14944585, essv14944546, essv14944547, essv14944588, essv14944623, essv14944601, essv14944619, essv14944626, essv14944562, essv14944549, essv14944614, essv14944574, essv14944559, essv14944580, essv14944627, essv14944616, essv14944540, essv14944552, essv14944551, essv14944620, essv14944570, essv14944548, essv14944578, essv14944550, essv14944617, essv14944568, essv14944589, essv14944583, essv14944539, essv14944603, essv14944587, essv14944556, essv14944572, essv14944600, essv14944608, essv14944590, essv14944592, essv14944573, essv14944610, essv14944569, essv14944581, essv14944609, essv14944596, essv14944599, essv14944595

Samples

NA19028, HG03366, HG01402, HG02652, HG01054, HG00231, HG04222, NA21099, HG00257, HG04164, NA20808, HG02734, HG04156, HG03235, NA19792, HG04100, HG03603, HG00122, NA20890, HG00689, HG04182, HG03885, HG02054, NA21103, HG04131, NA19384, HG03594, HG01859, NA18970, HG01067, NA20812, HG02597, NA11994, HG03744, HG02138, NA18990, HG01058, HG01121, HG03649, NA19027, HG00743, HG03862, NA19007, HG01353, HG01139, NA19082, HG01187, HG02793, HG02233, HG01384, HG04039, HG02025, NA20885, HG00732, HG02144, HG01323, HG01808, HG01447, HG01619, HG01870, HG01707, HG01613, HG01708, HG03006, HG01286, HG01204, HG04200, NA21143, NA18543, NA19747, HG01131, HG00734, HG02651, HG01396, HG02232, HG01798, NA19783, HG00125, NA19818, HG00478, NA19472, NA19779, HG01799, NA20758, HG01794, NA20886, HG02020, HG03698, NA20908, HG03989, HG03864

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3633821

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	91
Observed Complex	0
Frequency	n/a