View CNVs/SVs
View by Evidence Type: All (
CNVs Only Present In Patients
de novo CNVs
Overlapping/Recurrent CNVs
CNVs Overlapping With ACRD
CNVs Not Present In Control
Significant Enriched CNVs
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View by Chromosome:X ( 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 X Y All )
Notes: ACRD: Autism Chromosome Rearrangement Database
| CNV Name | Chr | Band | Gain/Loss | Number of CNVs | Evidence Type | Reference | |
|---|---|---|---|---|---|---|---|
| Case | Control | ||||||
| AutCNV0003056 | X | Xq23 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003057 | X | Xq23 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003058 | X | Xq23 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003059 | X | Xq23 | loss | 1 | - | Pinto, 2010 | |
| AutCNV0003060 | X | Xq24 | loss | 1 | - | Pinto, 2010 | |
| AutCNV0003061 | X | Xq25 | loss | 1 | - | Pinto, 2010 | |
| AutCNV0003062 | X | Xq26.3 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003063 | X | Xq26.3 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003064 | X | Xq26.3 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003065 | X | Xq26.3 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003066 | X | Xq27.1-27.2 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003067 | X | Xq27.1-27.2 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003068 | X | Xq27.2 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003069 | X | Xq27.2 | loss | 1 | - | Pinto, 2010 | |
| AutCNV0003070 | X | Xq27.2 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003071 | X | Xq27.3 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003072 | X | Xq27.3 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003073 | X | Xq27.3 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003074 | X | Xq28 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003075 | X | Xq28 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003076 | X | Xq28 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003077 | X | Xq28 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003078 | X | Xq28 | gain | 1 | - | Pinto, 2010 | |
| AutCNV0003118 | X | Xp11.22-p11.23 | gain | 1 | - | CNVs Only Present In Patients; | Chung, 2011 |
| AutCNV0003444 | X | Xp22.31 | gain | 1 | - | CNVs Only Present In Patients; | Gai, 2011 |