17q12, explained for kidsdeletion syndrome · static snapshot
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A number from a study What it can look like 1 supporting source confidence 80% novelty 60%

In one study of Müllerian aplasia, 4/63 cases (6 per cent) were linked to a 17q12 microdeletion

A source reports “63 cases” in the context of mullerian gu: “In one study of Müllerian aplasia, 4/63 cases (6 per cent) were linked to a 17q12 microdeletion.”

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How this was derived

Numbers are quoted verbatim from the source; check the source before quoting onward.

Generated 2026-11-13, last changed today. Dedup key freq:63 cases. The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.

Evidence (1 quote)

17q12 microdeletions (rarechromo.org patient leaflet) community · live page
In one study of Müllerian aplasia, 4/63 cases (6 per cent) were linked to a 17q12 microdeletion.

Supporting documents (1)

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17q12 microdeletions (rarechromo.org patient leaflet) patient_org - today 1.00