| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Callosome v0.587 | Sarah Milton Copied Region ISCA-37493-Loss from panel Common deletion and duplication syndromes | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Callosome v0.587 | ISCA-37493-Loss |
Sarah Milton Region: ISCA-37493-Loss was added Region: ISCA-37493-Loss was added to Callosome. Sources: Expert Review Green,Expert list SV/CNV tags were added to Region: ISCA-37493-Loss. Mode of inheritance for Region: ISCA-37493-Loss was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for Region: ISCA-37493-Loss were set to 28283832; 31929334; 31830750; 30853971 Phenotypes for Region: ISCA-37493-Loss were set to 1q43q44 microdeletion syndrome; intellectual disability; seizures; microcephaly; corpus callosum abnormalities |
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