Variant Details

Variant: esv2666019

Internal ID

9932124

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr10:114101962..114102271	hg38	UCSC Ensembl
	chr10:115861721..115862030	hg19	UCSC Ensembl

Cytoband

10q25.3

Allele length

Assembly	Allele length
hg38	310
hg19	310

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6065653, essv6576664, essv5618007, essv6590068, essv6346741, essv5632332, essv6466914, essv6459292, essv6357324, essv6348853, essv6145213, essv5506234, essv6265597, essv5985041, essv5709132, essv5592740, essv5412401, essv5645231, essv6378856, essv6335097, essv5827986, essv6546541, essv6229791, essv6175106, essv5941806, essv5842062, essv5780561, essv6433060, essv6429442, essv5591621, essv6362964, essv5735630, essv6587041, essv6506943, essv6517022, essv5621667, essv5699762, essv5435587, essv5635366, essv6252108, essv6544688, essv6033025, essv5942030, essv5737217, essv6366411, essv6408853, essv6367976, essv5806546, essv5688830, essv6318767, essv6333591, essv5551931, essv5921179, essv6325092, essv6134570, essv6179041, essv6473772, essv5934332, essv5918051, essv6068945, essv5531781, essv6121384, essv5933268, essv5913376, essv6306752, essv5478754, essv6545652, essv5691696, essv5519833, essv6357611, essv6229502, essv6273713, essv5416094, essv6059490, essv6032644, essv5789683, essv5533306, essv5856762, essv5747544, essv5493981, essv6288867, essv5774572, essv6366414, essv6027501, essv5836742, essv6459637, essv6249452, essv5503565, essv5410240, essv5638505, essv5696693, essv5396663, essv5714788, essv5621060, essv5985969, essv6018121, essv5709556, essv6476908, essv6173192, essv6023660, essv5631837, essv6049805, essv5692620, essv5624931, essv6215509, essv6134667, essv6035571, essv5855965, essv5997484, essv6151222, essv5957898, essv6354880, essv5551118, essv5739464, essv5729080, essv6239711, essv6015847, essv6000048, essv6595060, essv6125321, essv6447724, essv5826608, essv5765433, essv6404467, essv5412506, essv5565870, essv6428338, essv5849128, essv6217395, essv5909354, essv5684424, essv5876035, essv5577697, essv5463459, essv6448479, essv6557183, essv6013123, essv5761654, essv6595864, essv5959683, essv5535848, essv6085453, essv6020137, essv5475403, essv5895120, essv6136072, essv5849890, essv5481636, essv5581083, essv5708121, essv6490549, essv6584062, essv5641286, essv5438568, essv6259403, essv6170828, essv5756100, essv6535018, essv5453733, essv5996518, essv6312456, essv5692487, essv6256272, essv5547487, essv6507789, essv5500144, essv5408211, essv6580891, essv5884178, essv6257127, essv5725339, essv6473912, essv6312167, essv5959469, essv6547424, essv6465593, essv5905858, essv5928158, essv5468108, essv6003009, essv5675389, essv5574050, essv5562985, essv6054375, essv5938116, essv5881907, essv6470262, essv6450695, essv5612105, essv5769309, essv6295144, essv5960927, essv6322523, essv6198227, essv6198107, essv6373413, essv6471831, essv5557815, essv5508441, essv6209391, essv5664778, essv6060407, essv5543827, essv5929614, essv5836599, essv6298334, essv5707280, essv5441345, essv5647582, essv5473935

Samples

NA18502, HG01060, NA19648, HG01173, HG01098, NA19703, NA18924, NA19909, NA12286, HG00242, NA19204, NA18861, NA18508, NA18565, NA18507, NA11933, HG00257, HG01389, HG01066, NA18917, HG00318, NA19350, NA18486, HG00103, NA18504, NA20332, HG00737, HG00177, NA19443, NA19190, NA18870, HG01051, NA19920, NA18510, NA12750, HG01140, NA19107, NA19446, NA19374, HG00127, NA19373, NA19171, NA20796, NA18519, HG00122, NA18489, HG01351, HG00448, NA19119, NA18923, NA18635, NA19198, NA18567, NA18619, NA12348, HG01492, NA19131, NA18916, NA07048, NA19197, HG00346, HG01354, NA19457, NA19138, NA18498, HG01365, NA19130, NA20541, HG01134, HG00139, NA12282, NA12005, NA18874, HG00106, NA06984, HG01170, NA18868, NA19917, NA19137, NA11932, HG01072, NA19371, NA19731, NA11994, NA19235, NA19207, NA19172, NA19159, HG00427, NA19901, NA19189, NA18520, NA19239, HG01133, NA19209, HG00323, HG00253, NA19789, NA19200, NA19007, NA10847, HG00543, HG00133, HG01136, HG00188, HG00154, HG00268, HG00328, NA19152, NA18933, HG00732, NA20536, NA19236, NA18516, HG01498, NA19788, NA18579, NA20519, NA18910, NA18871, HG00740, NA18907, HG00324, HG00273, NA19461, NA19114, HG00651, NA19774, NA19655, HG00690, HG00404, HG00373, NA20581, HG00331, NA18499, NA18912, HG00117, NA19099, NA19257, HG00276, NA19225, NA20828, NA18523, NA19160, HG00246, NA18570, NA19625, NA18858, NA18608, NA19375, HG00611, NA20522, NA19440, NA12716, HG00254, NA18909, NA19834, NA19108, NA19147, NA19712, HG00366, HG00353, NA19072, HG00375, HG01551, HG00136, NA19240, HG00278, NA19144, NA12046, HG01375, NA19334, NA19439, NA20504, NA19311, HG01137, NA20803, NA07037, NA19818, NA19398, NA18501, HG00111, HG00513, NA19248, NA19223, HG00329, HG00342, NA20334, NA19093, HG00310, NA19102, NA18873, NA19770, HG00280, NA11843, NA20758, NA19780, NA19213, HG00274, HG01377, NA18505, NA19129, NA18488, NA20322, NA19463, NA18511, NA18522, HG01061, NA19153, NA18577

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2666019

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	210
Observed Complex	0
Frequency	n/a