@@ -1,5 +1,5 @@
<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
-<xs:schema xmlns:xs="http://www.w3.org/2001/XMLSchema" version="1.29; January 25, 2016">
+<xs:schema xmlns:xs="http://www.w3.org/2001/XMLSchema" version="1.27; December 29, 2015">
<xs:element name="ReleaseSet" type="ReleaseType"/>
<xs:element name="ClinVarSet" type="PublicSetType">
<xs:annotation>
@@ -421,13 +421,10 @@
<xs:enumeration value="CopyNumberTuple"/>
<xs:enumeration value="COSMIC"/>
<xs:enumeration value="SubmitterVariantId"/>
- <xs:enumeration value="ISCNCoordinates"/>
</xs:restriction>
</xs:simpleType>
</xs:attribute>
<xs:attribute name="Change" use="optional"/>
- <xs:attribute name="Accession" type="xs:string" use="optional"/>
- <xs:attribute name="Version" type="xs:positiveInteger" use="optional"/>
</xs:extension>
</xs:simpleContent>
</xs:complexType>
@@ -553,7 +550,6 @@
<xs:enumeration value="HGVS, non-validated"/>
<xs:enumeration value="HGVS, uncertain"/>
<xs:enumeration value="FunctionalConsequence"/>
- <xs:enumeration value="ISCNCoordinates"/>
</xs:restriction>
</xs:simpleType>
</xs:attribute>
@@ -1013,7 +1009,6 @@
<xs:enumeration value="NumberMosaic"/>
<xs:enumeration value="ObservedUnspecified"/>
<xs:enumeration value="AlleleFrequency"/>
- <xs:enumeration value="SecondaryFinding"/>
<xs:enumeration value="GenotypeAndMOIConsistent"/>
<xs:enumeration value="UnaffectedFamilyMemberWithCausativeVariant"/>
<xs:enumeration value="HetParentTransmitNormalAllele"/>