View CNVs/SVs
View by Evidence Type: Significant Enriched CNVs (
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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Notes: ACRD: Autism Chromosome Rearrangement Database
| CNV Name | Chr | Band | Gain/Loss | Number of CNVs | Evidence Type | Reference | |
|---|---|---|---|---|---|---|---|
| Case | Control | ||||||
| AutCNV0000358 | 7 | 7p21.2 | - | - | - | CNVs Only Present In Patients; Significant Enriched CNVs; | Zwaag, 2009 |
| AutCNV0000359 | 7 | 7q21.11 | - | - | - | CNVs Only Present In Patients; Significant Enriched CNVs; | Zwaag, 2009 |
| AutCNV0000360 | 7 | 7q22.3 | - | - | - | CNVs Only Present In Patients; Significant Enriched CNVs; | Zwaag, 2009 |
| AutCNV0004976 | 7 | 7q11.23 | - | - | - | CNVs Only Present In Patients; Significant Enriched CNVs; de novo CNVs; | Sanders SJ, 2015 |
| AutCNV0004977 | 7 | 7q11.23 | - | - | - | CNVs Only Present In Patients; Significant Enriched CNVs; de novo CNVs; | Sanders SJ, 2015 |
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