A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2744761



Internal ID10325731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:72135397..72181194hg38UCSC Ensembl
Outerchr11:71846443..71892238hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3845798
hg1945796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6938163, essv6681483, essv6953116, essv6763319, essv6916033, essv6870649, essv6891184, essv6743944, essv6698685, essv6920050, essv6907963, essv6791757, essv6743945, essv6752497, essv6684991, essv6806293, essv6672986, essv6851008, essv6804854, essv6681482, essv6746764, essv6800103, essv6775611, essv6887926, essv6827605, essv6691512, essv6812144, essv6970692, essv6720589, essv6864842, essv6857044, essv6812141, essv6755459, essv6787658, essv6706123, essv6900564, essv6894560, essv6737565, essv6706121, essv6873592, essv6851010, essv6812142, essv6803420, essv6695446, essv6908758, essv6823539, essv6864853, essv6838528, essv6931727, essv6920053, essv6672985, essv6887925, essv6845880, essv6709407, essv6862260, essv6706122, essv6965623, essv6809286, essv6771009, essv6885013, essv6970418, essv6908756, essv6867004, essv6765711, essv6791758, essv6783472, essv6959106, essv6867003, essv6879413, essv6891183, essv6760893, essv6779359, essv6710443, essv6948979, essv6873590, essv6800105, essv6800104, essv6760892, essv6870650, essv6712899, essv6938140, essv6940224, essv6842333, essv6940226, essv6787659, essv6712900, essv6904822, essv6867002, essv6749603, essv6720590, essv6768425, essv6688202, essv6976969, essv6779358, essv6953118, essv6823540, essv6879412, essv6724406, essv6953119, essv6876572, essv6710432, essv6944820, essv6740973, essv6702344, essv6842334, essv6831215, essv6815378, essv6716695, essv6691511, essv6965624, essv6882248, essv6959105, essv6681484, essv6728234, essv6809285, essv6938152, essv6795927, essv6749602, essv6686632, essv6882247, essv6803422, essv6891182, essv6827606, essv6834791, essv6677708, essv6920052, essv6873591, essv6898409, essv6714709, essv6775610, essv6737828, essv6908757, essv6936021, essv6940225, essv6677709, essv6924225, essv6834098, essv6698686
SamplesSSM100, SSM036, SSM008, SSM083, SSM071, SSM027, SSM024, SSM075, SSM045, SSM046, SSM011, SSM064, SSM079, SSM087, SSM038, SSM097, SSM039, SSM013, SSM009, SSM073, SSM093, SSM050, SSM074, SSM042, SSM088, SSM002, SSM041, SSM057, SSM023, SSM058, SSM028, SSM092, SSM084, SSM090, SSM021, SSM018, SSM069, SSM061, SSM029, SSM096, SSM062, SSM026, SSM089, SSM017, SSM035, SSM094, SSM032, SSM003, SSM031, SSM067, SSM044, SSM001, SSM014, SSM086, SSM033, SSM066, SSM006, SSM085, SSM068, SSM081, SSM040, SSM072, SSM082, SSM020, SSM007, SSM016, SSM053, SSM005, SSM080, SSM037, SSM077, SSM076, SSM022, SSM010, SSM091, SSM055, SSM070, SSM095, SSM025, SSM034, SSM004, SSM043, SSM052, SSM098, SSM056, SSM063, SSM012
Known GenesFOLR3
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2744761
Frequency
Sample Size96
Observed Gain0
Observed Loss87
Observed Complex0
Frequencyn/a


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