Variant DetailsVariant: esv2744662Internal ID | 9978946 | Landmark | | Location Information | | Cytoband | 11q13.2 | Allele length | Assembly | Allele length | hg38 | 128982 | hg19 | 128982 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6720582, essv6948970, essv6768415, essv6724398, essv6737824, essv6716683, essv6842325, essv6760885, essv6940213, essv6713709, essv6770954, essv6970679, essv6800097, essv6938085, essv6732019, essv6815368, essv6916028, essv6970362, essv6907917, essv6806290, essv6857030, essv6775604, essv6749595, essv6712886, essv6783461, essv6763316, essv6755456, essv6831205, essv6771957, essv6885009, essv6695437, essv6746755, essv6882245, essv6873585, essv6876567, essv6706113, essv6735105, essv6791751, essv6681473, essv6920036, essv6838524, essv6965613, essv6686576, essv6904809, essv6710421, essv6936009, essv6912487, essv6779348, essv6953105, essv6927834 | Samples | SSM008, SSM083, SSM027, SSM024, SSM045, SSM064, SSM065, SSM087, SSM013, SSM050, SSM074, SSM042, SSM002, SSM058, SSM028, SSM092, SSM084, SSM021, SSM047, SSM061, SSM062, SSM017, SSM019, SSM094, SSM003, SSM067, SSM044, SSM001, SSM033, SSM066, SSM006, SSM068, SSM081, SSM040, SSM072, SSM015, SSM016, SSM005, SSM037, SSM077, SSM022, SSM091, SSM055, SSM070, SSM095, SSM025, SSM004, SSM043, SSM049, SSM056 | Known Genes | PPP6R3 | 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) | esv2744662
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 50 | Observed Complex | 0 | Frequency | n/a |
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