Variant DetailsVariant: esv2747343Internal ID | 9981627 | Landmark | | Location Information | | Cytoband | 13q14.13 | Allele length | Assembly | Allele length | hg38 | 1086198 | hg19 | 1086198 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv223e201 | Supporting Variants | essv6862571, essv6920364, essv6949235, essv6779602, essv6916271, essv6749791, essv6900698, essv6815588, essv6819884, essv6823782, essv6809499, essv6966044, essv6912762, essv6977505, essv6882439, essv6691733, essv6716945, essv6746959, essv6738008, essv6685213, essv6953392, essv6775841, essv6966046, essv6773631, essv6966045, essv6940329, essv6755690, essv6807209, essv6953391, essv6720829, essv6775843, essv6851448, essv6787911, essv6796172, essv6803611, essv6851449, essv6876786, essv6835965, essv6772218, essv6912761, essv6720828, essv6823783, essv6744134, essv6959524, essv6773642, essv6758324, essv6909640, essv6928051, essv6713136, essv6959523, essv6741211, essv6783716, essv6755689, essv6761081, essv6763488, essv6668300, essv6835954, essv6716946, essv6827879, essv6838763, essv6932009, essv6977504, essv6681729, essv6673392, essv6819883, essv6752674, essv6940340, essv6755691, essv6905046, essv6900739, essv6936309, essv6728472, essv6920365, essv6735295, essv6857446, essv6691734, essv6779601, essv6894789, essv6873796, essv6819882, essv6724640, essv6970983, essv6842593, essv6735296, essv6765860, essv6966043, essv6768625, essv6867350, essv6928053, essv6831458, essv6712077, essv6739553, essv6712066 | Samples | SSM100, SSM059, SSM036, SSM008, SSM083, SSM071, SSM027, SSM024, SSM075, SSM045, SSM046, SSM064, SSM079, SSM065, SSM087, SSM013, SSM009, SSM073, SSM050, SSM042, SSM088, SSM002, SSM057, SSM058, SSM028, SSM092, SSM084, SSM021, SSM069, SSM061, SSM029, SSM062, SSM026, SSM089, SSM017, SSM019, SSM094, SSM003, SSM031, SSM067, SSM044, SSM086, SSM033, SSM066, SSM006, SSM068, SSM081, SSM020, SSM007, SSM015, SSM078, SSM016, SSM053, SSM080, SSM077, SSM010, SSM091, SSM055, SSM025, SSM034, SSM043, SSM052, SSM098, SSM049, SSM056, SSM030, SSM063, SSM012 | Known Genes | COG3, CPB2, CPB2-AS1, FAM194B, KIAA0226L, LCP1, LINC00563, LRRC63, SIAH3, SLC25A30, SPERT, TPT1-AS1, ZC3H13 | Method | Sequencing | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | Platform | Illumina HiSeq 2000 | Comments | | Reference | Wong_et_al_2012b | Pubmed ID | 23290073 | Accession Number(s) | esv2747343
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 68 | Observed Complex | 0 | Frequency | n/a |
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