Variant Details

Variant: esv2661497

Internal ID

9927602

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr14:52290064..52290395	hg38	UCSC Ensembl
	chr14:52756782..52757113	hg19	UCSC Ensembl

Cytoband

14q22.1

Allele length

Assembly	Allele length
hg38	332
hg19	332

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5953990, essv5602603, essv6155799, essv5851554, essv6474397, essv6399612, essv6368272, essv6494212, essv6028202, essv6499677, essv6249616, essv6509264, essv6503361, essv5822623, essv6007235, essv5401202, essv6546972, essv6378343, essv6272083, essv6084198, essv6042808, essv5954340, essv6471327, essv6443712, essv5584609, essv5636302, essv5747719, essv5557941, essv5460261, essv6512941, essv6032080, essv5769731, essv5720859, essv5840561, essv5660340, essv6578945, essv6373168, essv5582078, essv5594509, essv5912471, essv6383587, essv5527507, essv5424996, essv6568835, essv6255069, essv5802161, essv5962241, essv6233176, essv6104181, essv5952473, essv6311579, essv6032196, essv6020914, essv6576468, essv6527399, essv6333574, essv6253658, essv5856495, essv6325921, essv5664294, essv6595891, essv5515176, essv6447867, essv6001236, essv6173729, essv6006294, essv5546680, essv5844917, essv5810409, essv6595964, essv6388115, essv6597615, essv6261090, essv6195420, essv6101143, essv5957818, essv5911346, essv6144785, essv5749130, essv6308477, essv6557330, essv6125837, essv6293721, essv6116713, essv5495602, essv5534183, essv6467310, essv5623633, essv5657914, essv6329464, essv6567049, essv6391478, essv5832780, essv5804572, essv6065192, essv5441487, essv6175039, essv5797065, essv5658049, essv5469947, essv5437001, essv6050143, essv5549905, essv6088973, essv5632885, essv6340061, essv6572310, essv6356342, essv6222164, essv6005018, essv5938683, essv5916996, essv6465066, essv6499682, essv6161445, essv6337440, essv6074580, essv5689355, essv5828223, essv5811304, essv5612819, essv5913557, essv5653900, essv5606546, essv5979127, essv6573184, essv6018929, essv5659872, essv5461259, essv5685927, essv6077601, essv5943198, essv6142845, essv5580295, essv5565813, essv5923845, essv6161040, essv6027296, essv5570261, essv6081402, essv6175480, essv5661616, essv6575075, essv6530941, essv6204774, essv5456370, essv5934427, essv6554710, essv5633358, essv5561190, essv5548911, essv5456814

Samples

NA19394, NA19701, HG00650, NA19700, HG01356, HG00143, NA19703, NA19397, NA18924, NA19909, NA19664, NA11829, NA19204, NA19399, NA12414, NA18980, NA18507, NA20531, NA18917, NA19359, NA19092, NA18486, NA19819, NA19393, NA18959, NA18616, HG00177, NA19443, NA19190, NA19098, NA18870, NA18510, NA18602, HG00327, NA12813, NA19446, NA18967, NA07346, NA19396, NA19171, NA18944, NA19319, NA19201, NA18489, NA19448, NA20586, NA19119, NA18923, NA20317, NA19916, NA19131, NA19197, NA11918, NA18498, NA18874, NA12156, HG01495, NA19137, HG01072, HG00232, NA19372, NA19371, NA19238, NA19235, NA19207, NA19471, NA19159, NA19189, NA18520, NA19239, NA18557, NA19209, NA18975, NA18908, NA19200, NA19007, NA19908, NA19210, HG00596, NA19462, NA19152, NA18933, HG00577, NA19391, NA19455, NA18516, NA19982, HG00584, NA18910, NA18871, NA18976, NA18981, HG00273, NA19461, NA19114, HG00404, NA18499, NA18856, NA18912, NA18532, HG01101, NA19338, NA19257, NA18555, NA19452, NA19160, NA20542, NA18858, NA18974, NA20296, NA18953, NA19375, NA19390, HG00336, NA19321, NA19108, NA19256, NA19147, NA18517, NA20276, NA18564, NA19240, NA19144, NA19439, NA19470, NA19428, NA19311, HG00256, NA12763, HG01342, HG00339, HG00269, NA19376, NA06994, NA20348, NA19785, NA18971, NA20334, NA19468, NA19713, NA19093, NA18873, NA19116, NA18972, NA19900, NA18505, NA19129, NA20322, NA18968, NA18511, NA12154, NA19153

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2661497

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	152
Observed Complex	0
Frequency	n/a