Denovo refers to a genetic variant that arises spontaneously in an individual, not inherited from either parent. It is identified through advanced genomic sequencing, often comparing a child’s DNA against both parents. This analysis is crucial for diagnosing rare developmental disorders, intellectual disabilities, or congenital anomalies. Families, genetic counselors, and researchers benefit most, as Denovo findings clarify disease causes, guide management, and inform recurrence risks for future pregnancies.
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