The Chromosome 7 Annotation Project

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breaktype		uniqueid
Karyotype	46, XX, inv(7)(q11.23q21.3) de novo. WBSinv-1 [detected by FISH]	Phenotype	ectrodactyly, WBS facies, developmental delay, strabismus, WBS-like behaviour profile, lordosis, chronic otitis media, normal growth, inattention
cytogen_from		cytogen_to
molecular_1		molecular_2
Pubmed ID		patientid
Comments
Comments	Non Malignant Malignant
Old Molecular_1	AC067941/ AC005074	Old Molecular_2	AZ757826/ AZ757825
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