Variant DetailsVariant: esv2745657 Internal ID | 9979941 | Landmark | | Location Information | | Cytoband | 12p11.23 | Allele length | Assembly | Allele length | hg38 | 311 | hg19 | 311 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6809377, essv6977177, essv6673146, essv6862374, essv6857192, essv6677812, essv6702449, essv6851174, essv6867152, essv6685078, essv6779458, essv6894639, essv6838622, essv6803508, essv6965768, essv6891278, essv6885084, essv6959258, essv6688287, essv6709491, essv6908874, essv6819684, essv6865621, essv6812215, essv6944951, essv6823619, essv6728328, essv6900645 | Samples | SSM100, SSM083, SSM027, SSM075, SSM046, SSM011, SSM079, SSM087, SSM097, SSM039, SSM073, SSM088, SSM041, SSM023, SSM029, SSM026, SSM089, SSM035, SSM032, SSM031, SSM067, SSM014, SSM086, SSM078, SSM076, SSM095, SSM034, SSM098 | Known Genes | ITPR2 | 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) | esv2745657
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 28 | Observed Complex | 0 | Frequency | n/a |
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